A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615402



Internal ID16056125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128688946..128690282hg38UCSC Ensembl
Innerchr9:131451225..131452561hg19UCSC Ensembl
Innerchr9:130491046..130492382hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381337
hg191337
hg181337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12884n54
Supporting Variantsnssv1143248, nssv1143247, nssv1143249
Samples
Known GenesSET
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615402
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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