A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615289



Internal ID16402698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124298152..124355067hg38UCSC Ensembl
Innerchr9:127060431..127117346hg19UCSC Ensembl
Innerchr9:126100252..126157167hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3856916
hg1956916
hg1856916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12866n54
Supporting Variantsnssv1141317
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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