A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614733



Internal ID16055456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78028462..78032086hg38UCSC Ensembl
Innerchr9:80643378..80647002hg19UCSC Ensembl
Innerchr9:79833198..79836822hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg383625
hg193625
hg183625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137704
Samples
Known GenesGNAQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614733
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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