A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624328



Internal ID6664495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97983247..97983584hg38UCSC Ensembl
Innerchr10:97983248..97983584hg38UCSC Ensembl
Outerchr10:97983247..97983585hg38UCSC Ensembl
chr10:99743004..99743341hg19UCSC Ensembl
Innerchr10:99743005..99743341hg19UCSC Ensembl
Outerchr10:99743004..99743342hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13908965, essv13908964, essv13908999, essv13908953, essv13908944, essv13908950, essv13908986, essv13909021, essv13908978, essv13909008, essv13908952, essv13908947, essv13908957, essv13908997, essv13908955, essv13908975, essv13909015, essv13908976, essv13908961, essv13908942, essv13908951, essv13909016, essv13908960, essv13908984, essv13908982, essv13909000, essv13908968, essv13908998, essv13908943, essv13909014, essv13908949, essv13908979, essv13908983, essv13909013, essv13908946, essv13908981, essv13908963, essv13908993, essv13909005, essv13908989, essv13908994, essv13909004, essv13908996, essv13908980, essv13908990, essv13909001, essv13909007, essv13908959, essv13908956, essv13908977, essv13908987, essv13908945, essv13908971, essv13908988, essv13908969, essv13909017, essv13909010, essv13909012, essv13908972, essv13909018, essv13908985, essv13909024, essv13908967, essv13908995, essv13908974, essv13909002, essv13909020, essv13909023, essv13908970, essv13909011, essv13908991, essv13909003, essv13909006, essv13908962, essv13908954, essv13909009, essv13908948, essv13908958, essv13908992, essv13908966, essv13908973, essv13909019, essv13909022
SamplesHG02715, HG02580, NA19913, HG02107, HG02477, HG02854, HG03120, NA18861, HG02882, NA19904, HG03064, HG03382, NA19819, HG01064, HG01882, NA19209, HG03410, HG03452, HG03469, HG02722, HG02322, NA19378, HG03548, NA18488, HG03039, HG03572, HG03049, HG02982, HG02588, HG03451, HG02646, HG02703, HG03436, NA19397, HG03052, HG03539, HG03027, NA19324, HG03225, HG02840, NA19153, NA19129, HG02537, HG02768, HG03040, NA19393, NA18510, HG03472, HG02573, HG01889, HG02511, HG02771, NA18878, HG02307, HG02545, HG02571, HG02052, HG03577, HG03115, HG02339, HG02624, HG02881, HG03028, HG03224, NA19138, NA18907, NA18909, NA20332, NA19394, HG02465, HG02679, HG03369, HG01912, HG03270, HG03271, HG02798, HG02620, HG03515, HG02013, HG02860, HG03460, HG02769, NA19922
Known GenesCRTAC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624328
Frequency
Sample Size2504
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer