A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13515769



Internal ID5765067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72064216..72074787hg38UCSC Ensembl
chr9:74679132..74689703hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810572
hg1910572
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620623
Supporting Variants
SamplesNA19137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13515769
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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