A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624803



Internal ID7011653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123982697..123984810hg38UCSC Ensembl
Innerchr10:123982697..123984810hg38UCSC Ensembl
Outerchr10:123982570..123984952hg38UCSC Ensembl
chr10:125742213..125744326hg19UCSC Ensembl
Innerchr10:125742213..125744326hg19UCSC Ensembl
Outerchr10:125742086..125744468hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382114
hg192114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963162, essv13963163, essv13963161
SamplesHG00108, NA11831, HG00278
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624803
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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