A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523169



Internal ID15103776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72886525..73255193hg38UCSC Ensembl
Innerchr4:73752242..74120910hg19UCSC Ensembl
Innerchr4:73971106..74339774hg18UCSC Ensembl
Innerchr4:74117277..74485945hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38368669
hg19368669
hg18368669
hg17368669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698881
Samples
Known GenesANKRD17, COX18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523169
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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