A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525215



Internal ID15452508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45353098..45372288hg38UCSC Ensembl
Innerchr4:45355115..45374305hg19UCSC Ensembl
Innerchr4:45049872..45069062hg18UCSC Ensembl
Innerchr4:45196043..45215233hg17UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3819191
hg1919191
hg1819191
hg1719191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701298
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525215
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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