A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524222



Internal ID15451515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105504357..105544717hg38UCSC Ensembl
Innerchr13:106156706..106197066hg19UCSC Ensembl
Innerchr13:104954707..104995067hg18UCSC Ensembl
Innerchr13:104954707..104995067hg17UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3840361
hg1940361
hg1840361
hg1740361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700110
Samples
Known GenesDAOA-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524222
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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