A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528687



Internal ID15109294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:132750285..132779155hg38UCSC Ensembl
Innerchr5:132085977..132114847hg19UCSC Ensembl
Innerchr5:132113876..132142746hg18UCSC Ensembl
Innerchr5:132113876..132142746hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3828871
hg1928871
hg1828871
hg1728871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705330
Samples
Known GenesCCNI2, SEPT8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528687
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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