A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614209



Internal ID16401618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36487307..36488025hg38UCSC Ensembl
Innerchr9:36487304..36488022hg19UCSC Ensembl
Innerchr9:36477304..36478022hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38719
hg19719
hg18719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12669n54
Supporting Variantsnssv1133968
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614209
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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