A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615934



Internal ID16403343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135906649..135908168hg38UCSC Ensembl
Innerchr9:138798495..138800014hg19UCSC Ensembl
Innerchr9:137938316..137939835hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381520
hg191520
hg181520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12997n54
Supporting Variantsnssv1148262
Samples
Known GenesCAMSAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615934
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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