A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619992



Internal ID7006865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22696399..22740886hg38UCSC Ensembl
Innerchr9:22696399..22740886hg38UCSC Ensembl
Outerchr9:22695899..22741386hg38UCSC Ensembl
chr9:22696398..22740885hg19UCSC Ensembl
Innerchr9:22696398..22740885hg19UCSC Ensembl
Outerchr9:22695898..22741385hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3844488
hg1944488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13426170
SamplesNA20807
Known GenesFLJ35282
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619992
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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