A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615933



Internal ID16403342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135906649..135907886hg38UCSC Ensembl
Innerchr9:138798495..138799732hg19UCSC Ensembl
Innerchr9:137938316..137939553hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381238
hg191238
hg181238
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12997n54
Supporting Variantsnssv1148261
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615933
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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