A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176517



Internal ID15527794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133156364..133290774hg38UCSC Ensembl
Innerchr9:136031751..136166346hg19UCSC Ensembl
Innerchr9:135021572..135156167hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38134411
hg19134596
hg18134596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615612
Supporting Variants
SamplesHGDP00545
Known GenesABO, GBGT1, OBP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176517
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer