A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614742



Internal ID16055465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78031325..78032360hg38UCSC Ensembl
Innerchr9:80646241..80647276hg19UCSC Ensembl
Innerchr9:79836061..79837096hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381036
hg191036
hg181036
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12773n54
Supporting Variantsnssv1137718, nssv1137719
Samples
Known GenesGNAQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614742
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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