A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141450



Internal ID15647950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127091920..127178137hg38UCSC Ensembl
Innerchr9:129854199..129940416hg19UCSC Ensembl
Innerchr9:128894020..128980237hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3886218
hg1986218
hg1886218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615342
Supporting Variants
Samples
Known GenesANGPTL2, RALGPS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141450
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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