A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519151



Internal ID15099758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3374106..3420366hg38UCSC Ensembl
Innerchr7:3413738..3459998hg19UCSC Ensembl
Innerchr7:3380264..3426524hg18UCSC Ensembl
Innerchr7:3186979..3233239hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3846261
hg1946261
hg1846261
hg1746261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696628
Samples
Known GenesSDK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519151
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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