A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521630



Internal ID15448923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9916121..10165287hg38UCSC Ensembl
Innerchr7:9955750..10204914hg19UCSC Ensembl
Innerchr7:9922275..10171439hg18UCSC Ensembl
Innerchr7:9728990..9978154hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38249167
hg19249165
hg18249165
hg17249165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698249
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521630
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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