A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519767



Internal ID15100374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124247983..124364893hg38UCSC Ensembl
Innerchr9:127010262..127127172hg19UCSC Ensembl
Innerchr9:126050083..126166993hg18UCSC Ensembl
Innerchr9:124089816..124206726hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38116911
hg19116911
hg18116911
hg17116911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692234, nssv688352, nssv658400, nssv685856, nssv660877, nssv679769, nssv674014, nssv683298, nssv683358
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519767
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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