A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13685657



Internal ID5822914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5609236..5660606hg38UCSC Ensembl
chr10:5651199..5702569hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851371
hg1951371
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622232
Supporting Variants
SamplesNA19200
Known GenesASB13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13685657
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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