A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525121



Internal ID15452414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:28838993..28870396hg38UCSC Ensembl
Innerchr5:28839100..28870503hg19UCSC Ensembl
Innerchr5:28874857..28906260hg18UCSC Ensembl
Innerchr5:28874857..28906260hg17UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3831404
hg1931404
hg1831404
hg1731404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701189
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525121
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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