A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679769



Internal ID15069735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:124247983..124328687hg38UCSC Ensembl
Innerchr9:127010262..127090966hg19UCSC Ensembl
Innerchr9:126050083..126130787hg18UCSC Ensembl
Innerchr9:124089816..124170520hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3880705
hg1980705
hg1880705
hg1780705
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519767
Supporting Variants
Samples
Known GenesNEK6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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