A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13665663



Internal ID3667479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1514571..1515004hg38UCSC Ensembl
Innerchr10:1514575..1515000hg38UCSC Ensembl
Outerchr10:1514567..1515008hg38UCSC Ensembl
chr10:1556766..1557199hg19UCSC Ensembl
Innerchr10:1556770..1557195hg19UCSC Ensembl
Outerchr10:1556762..1557203hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622103
Supporting Variants
SamplesHG01597
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13665663
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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