A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615932



Internal ID16403341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135905450..135908222hg38UCSC Ensembl
Innerchr9:138797296..138800068hg19UCSC Ensembl
Innerchr9:137937117..137939889hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382773
hg192773
hg182773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12996n54
Supporting Variantsnssv1148260, nssv1148259
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615932
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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