A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13687154



Internal ID6301440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5861771..5864739hg38UCSC Ensembl
Innerchr10:5861788..5864722hg38UCSC Ensembl
Outerchr10:5861754..5864756hg38UCSC Ensembl
chr10:5903734..5906702hg19UCSC Ensembl
Innerchr10:5903751..5906685hg19UCSC Ensembl
Outerchr10:5903717..5906719hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622238
Supporting Variants
SamplesNA19904
Known GenesANKRD16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13687154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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