A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622822



Internal ID7009680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31984844..31994009hg38UCSC Ensembl
Innerchr10:31984877..31993977hg38UCSC Ensembl
Outerchr10:31984812..31994042hg38UCSC Ensembl
chr10:32273772..32282937hg19UCSC Ensembl
Innerchr10:32273805..32282905hg19UCSC Ensembl
Outerchr10:32273740..32282970hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg389166
hg199166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv107e214
Supporting Variantsessv13749847, essv13749848
SamplesHG02496, HG01122
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622822
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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