A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615937



Internal ID16403346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135906813..135908114hg38UCSC Ensembl
Innerchr9:138798659..138799960hg19UCSC Ensembl
Innerchr9:137938480..137939781hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381302
hg191302
hg181302
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12998n54
Supporting Variantsnssv1148272, nssv1148271, nssv1148270
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615937
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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