A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615277



Internal ID16402686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123346788..123351315hg38UCSC Ensembl
Innerchr9:126109067..126113594hg19UCSC Ensembl
Innerchr9:125148888..125153415hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384528
hg194528
hg184528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141304
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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