A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685856



Internal ID15075822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124298152..124364893hg38UCSC Ensembl
Innerchr9:127060431..127127172hg19UCSC Ensembl
Innerchr9:126100252..126166993hg18UCSC Ensembl
Innerchr9:124139985..124206726hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3866742
hg1966742
hg1866742
hg1766742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519767
Supporting Variants
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685856
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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