A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622102



Internal ID6662272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1398165..1410802hg38UCSC Ensembl
Innerchr10:1398170..1410798hg38UCSC Ensembl
Outerchr10:1398161..1410807hg38UCSC Ensembl
chr10:1440360..1452997hg19UCSC Ensembl
Innerchr10:1440365..1452993hg19UCSC Ensembl
Outerchr10:1440356..1453002hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3812638
hg1912638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13665659, essv13665658, essv13665660
SamplesNA12814, HG00114, HG00142
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622102
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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