A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528971



Internal ID15456264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3548632..3556146hg38UCSC Ensembl
Innerchr5:3548746..3556260hg19UCSC Ensembl
Innerchr5:3601746..3609260hg18UCSC Ensembl
Innerchr5:3601746..3609260hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg387515
hg197515
hg187515
hg177515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705670
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528971
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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