A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699615



Internal ID15436267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7064934..7075305hg38UCSC Ensembl
Innerchr9:7064934..7075305hg19UCSC Ensembl
Innerchr9:7054934..7065305hg18UCSC Ensembl
Innerchr9:7054934..7065305hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3810372
hg1910372
hg1810372
hg1710372
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523788
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699615
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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