A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137713



Internal ID15644213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:78031000..78032360hg38UCSC Ensembl
Innerchr9:80645916..80647276hg19UCSC Ensembl
Innerchr9:79835736..79837096hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381361
hg191361
hg181361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614740
Supporting Variants
Samples
Known GenesGNAQ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137713
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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