A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521304



Internal ID15448597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10710604..10727527hg38UCSC Ensembl
Innerchr5:10710716..10727639hg19UCSC Ensembl
Innerchr5:10763716..10780639hg18UCSC Ensembl
Innerchr5:10763716..10780639hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3816924
hg1916924
hg1816924
hg1716924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697910
Samples
Known GenesDAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521304
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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