A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519175



Internal ID15446468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108331662..108339325hg38UCSC Ensembl
Innerchr13:108984010..108991673hg19UCSC Ensembl
Innerchr13:107782011..107789674hg18UCSC Ensembl
Innerchr13:107782011..107789674hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg387664
hg197664
hg187664
hg177664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv119n21
Supporting Variantsnssv696658
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519175
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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