A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623868



Internal ID7010724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76619034..76621077hg38UCSC Ensembl
Innerchr10:76619069..76621043hg38UCSC Ensembl
Outerchr10:76619000..76621112hg38UCSC Ensembl
chr10:78378792..78380835hg19UCSC Ensembl
Innerchr10:78378827..78380801hg19UCSC Ensembl
Outerchr10:78378758..78380870hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382044
hg192044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13866382, essv13866376, essv13866375, essv13866372, essv13866373, essv13866378, essv13866371, essv13866379, essv13866374, essv13866381, essv13866377, essv13866380
SamplesHG03378, NA19204, HG02702, HG03115, HG03193, HG02810, HG02541, NA19159, HG02879, HG02508, NA19713, HG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623868
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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