A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698108



Internal ID15434760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4253892..4254344hg38UCSC Ensembl
Innerchr7:4293524..4293976hg19UCSC Ensembl
Innerchr7:4260050..4260502hg18UCSC Ensembl
Innerchr7:4066765..4067217hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38453
hg19453
hg18453
hg17453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517675
Supporting Variants
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698108
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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