A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615691



Internal ID16403100
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 StatusM
Merged Variants
Supporting Variantsnssv1176523
SamplesHGDP00244
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615691
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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