A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13713844



Internal ID4759359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20492763..20534910hg38UCSC Ensembl
chr10:20781692..20823839hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3842148
hg1942148
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622556
Supporting Variants
SamplesNA11829
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13713844
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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