A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524103



Internal ID15451396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:74194739..74210286hg38UCSC Ensembl
Innerchr5:73490564..73506111hg19UCSC Ensembl
Innerchr5:73526320..73541867hg18UCSC Ensembl
Innerchr5:73526320..73541867hg17UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3815548
hg1915548
hg1815548
hg1715548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv345n21
Supporting Variantsnssv699978
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524103
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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