A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620763



Internal ID7007633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77086677..77090072hg38UCSC Ensembl
chr9:79701593..79704988hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg383396
hg193396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13531726, essv13531729, essv13531728, essv13531727
SamplesNA19471, HG01988, HG03695, NA19328
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620763
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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