A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527787



Internal ID15455080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74376396..74409017hg38UCSC Ensembl
Innerchr13:74950533..74983154hg19UCSC Ensembl
Innerchr13:73848534..73881155hg18UCSC Ensembl
Innerchr13:73848534..73881155hg17UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3832622
hg1932622
hg1832622
hg1732622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv113n21
Supporting Variantsnssv704278
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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