A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526962



Internal ID15454255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83950475..83985680hg38UCSC Ensembl
Innerchr13:84524610..84559815hg19UCSC Ensembl
Innerchr13:83422611..83457816hg18UCSC Ensembl
Innerchr13:83422611..83457816hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3835206
hg1935206
hg1835206
hg1735206
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703334
Samples
Known GenesMIR548F1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526962
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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