A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622902



Internal ID6663071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35606270..35610297hg38UCSC Ensembl
Innerchr10:35606280..35610287hg38UCSC Ensembl
Outerchr10:35606260..35610307hg38UCSC Ensembl
chr10:35895198..35899225hg19UCSC Ensembl
Innerchr10:35895208..35899215hg19UCSC Ensembl
Outerchr10:35895188..35899235hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384028
hg194028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13752309, essv13752310, essv13752311
SamplesNA19030, HG03521, NA19819
Known GenesGJD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622902
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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