A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705365



Internal ID15442017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3411619..3558949hg38UCSC Ensembl
Innerchr7:3451251..3598581hg19UCSC Ensembl
Innerchr7:3417777..3565107hg18UCSC Ensembl
Innerchr7:3224492..3371822hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38147331
hg19147331
hg18147331
hg17147331
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528715
Supporting Variants
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705365
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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