A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525135



Internal ID15452428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7953761..7957302hg38UCSC Ensembl
Innerchr4:7955488..7959029hg19UCSC Ensembl
Innerchr4:8006388..8009929hg18UCSC Ensembl
Innerchr4:8073559..8077100hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg383542
hg193542
hg183542
hg173542
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701205
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525135
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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