A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662173



Internal ID9928278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98026154..98028110hg38UCSC Ensembl
Outerchr7:98025733..98028480hg38UCSC Ensembl
Innerchr7:97655466..97657422hg19UCSC Ensembl
Outerchr7:97655045..97657792hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382748
hg192748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5438255, essv6395251, essv5958223, essv6398136, essv6302556, essv5894244, essv6522519, essv6288942, essv5976937, essv6171363, essv5464669, essv5676108, essv6010794, essv6353380, essv5553827, essv6291045, essv6174562, essv5885869, essv6369938, essv6495086, essv5659723, essv6167090, essv6292887, essv6443603, essv5871727, essv5760924, essv5828080, essv6364372, essv6489570, essv5475619, essv5981290, essv6229903, essv5673893, essv5396971, essv5931318, essv6221393, essv6193878, essv6157014, essv6152729, essv6462768, essv5534075, essv6577553
SamplesNA18947, NA19066, NA18980, NA18999, NA18959, NA19068, NA18940, NA18982, NA19782, NA19681, NA19079, NA18949, NA19720, NA19731, NA18973, NA19789, NA18951, NA19070, NA18956, NA19663, NA19081, NA19788, NA18948, NA19761, NA19682, NA18961, NA18952, NA19749, NA19747, NA19072, NA18941, NA19083, NA19783, NA19085, NA19060, NA19770, NA19080, NA19780, NA18972, NA19661, NA19065, NA18965
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662173
Frequency
Sample Size1151
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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