A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519189



Internal ID15446482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148559462..148583613hg38UCSC Ensembl
Innerchr7:148256554..148280705hg19UCSC Ensembl
Innerchr7:147887487..147911638hg18UCSC Ensembl
Innerchr7:147694202..147718353hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3824152
hg1924152
hg1824152
hg1724152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694314
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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