A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13665706



Internal ID3667522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1588970..1596831hg38UCSC Ensembl
Innerchr10:1588970..1596831hg38UCSC Ensembl
Outerchr10:1588470..1597331hg38UCSC Ensembl
chr10:1631165..1639026hg19UCSC Ensembl
Innerchr10:1631165..1639026hg19UCSC Ensembl
Outerchr10:1630665..1639526hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg387862
hg197862
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622108
Supporting Variants
SamplesNA18582
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13665706
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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