A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614208



Internal ID16401617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36487248..36488264hg38UCSC Ensembl
Innerchr9:36487245..36488261hg19UCSC Ensembl
Innerchr9:36477245..36478261hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg381017
hg191017
hg181017
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12673n54
Supporting Variantsnssv1133966, nssv1133967
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614208
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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