A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620634



Internal ID7007504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72370141..72377646hg38UCSC Ensembl
chr9:74985057..74992562hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387506
hg197506
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13516174, essv13516173, essv13516172, essv13516171
SamplesHG03792, HG01565, NA21143, HG03695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620634
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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