A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176523



Internal ID15873575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133752170..133793694hg38UCSC Ensembl
Innerchr9:136617292..136658816hg19UCSC Ensembl
Innerchr9:135607113..135648637hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3841525
hg1941525
hg1841525
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615691
Supporting Variants
SamplesHGDP00244
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176523
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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