A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622203



Internal ID7009062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4644851..4645464hg38UCSC Ensembl
Innerchr10:4644851..4645464hg38UCSC Ensembl
Outerchr10:4644572..4645721hg38UCSC Ensembl
chr10:4687043..4687656hg19UCSC Ensembl
Innerchr10:4687043..4687656hg19UCSC Ensembl
Outerchr10:4686764..4687913hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13683018, essv13683003, essv13683015, essv13683021, essv13683023, essv13683020, essv13683011, essv13683009, essv13683006, essv13683008, essv13682999, essv13683005, essv13683004, essv13683013, essv13683019, essv13683016, essv13683012, essv13683010, essv13683022, essv13683007, essv13683000, essv13683014, essv13683002, essv13682998, essv13682997, essv13683001, essv13683017
SamplesHG02339, NA19397, NA18508, NA18507, NA18877, NA18878, HG02536, NA18519, HG03168, NA18498, HG03268, HG02946, NA20127, NA19210, HG02554, HG02014, HG02586, HG03108, HG02771, NA20357, NA19143, NA19185, NA19711, NA18511, HG03303, HG03129, NA19346
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622203
Frequency
Sample Size2504
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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