A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614952



Internal ID16402361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98600551..98657550hg38UCSC Ensembl
Innerchr9:101362833..101419832hg19UCSC Ensembl
Innerchr9:100402654..100459653hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3857000
hg1957000
hg1857000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176002
Samples1780854419_A
Known GenesGABBR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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