A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615939



Internal ID16403348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135906813..135908222hg38UCSC Ensembl
Innerchr9:138798659..138800068hg19UCSC Ensembl
Innerchr9:137938480..137939889hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381410
hg191410
hg181410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12997n54
Supporting Variantsnssv1148280, nssv1148277, nssv1148278, nssv1148274, nssv1148279, nssv1148275, nssv1148276
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615939
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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