A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620622



Internal ID7007492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72064216..72074787hg38UCSC Ensembl
chr9:74679132..74689703hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810572
hg1910572
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13515761, essv13515765, essv13515766, essv13515768, essv13515762, essv13515763, essv13515767, essv13515764
SamplesNA12842, HG01305, NA12340, HG01058, NA12718, HG01047, HG01197, HG01108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620622
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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