A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521853



Internal ID15449146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19287465..19320159hg38UCSC Ensembl
Innerchr7:19327088..19359782hg19UCSC Ensembl
Innerchr7:19293613..19326307hg18UCSC Ensembl
Innerchr7:19100328..19133022hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3832695
hg1932695
hg1832695
hg1732695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694627
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521853
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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