A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614950



Internal ID16402359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98583496..98600551hg38UCSC Ensembl
Innerchr9:101345778..101362833hg19UCSC Ensembl
Innerchr9:100385599..100402654hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3817056
hg1917056
hg1817056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140213
Samples
Known GenesGABBR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614950
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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