A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528664



Internal ID15109271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22001786..22062834hg38UCSC Ensembl
Innerchr1:22328279..22389327hg19UCSC Ensembl
Innerchr1:22200866..22261914hg18UCSC Ensembl
Innerchr1:22073585..22134633hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3861049
hg1961049
hg1861049
hg1761049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705302
Samples
Known GenesCDC42, CELA3A, LINC00339
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528664
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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