A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524788



Internal ID15105395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:44918011..44966001hg38UCSC Ensembl
Innerchr13:45492146..45540136hg19UCSC Ensembl
Innerchr13:44390146..44438136hg18UCSC Ensembl
Innerchr13:44390146..44438136hg17UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3847991
hg1947991
hg1847991
hg1747991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700780
Samples
Known GenesNUFIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524788
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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