A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519024



Internal ID15446317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19064303..19094496hg38UCSC Ensembl
Innerchr7:19103926..19134119hg19UCSC Ensembl
Innerchr7:19070451..19100644hg18UCSC Ensembl
Innerchr7:18877166..18907359hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3830194
hg1930194
hg1830194
hg1730194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696493
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519024
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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