A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518074



Internal ID15445367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51111653..51116248hg38UCSC Ensembl
Innerchr13:51685789..51690384hg19UCSC Ensembl
Innerchr13:50583790..50588385hg18UCSC Ensembl
Innerchr13:50583790..50588385hg17UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384596
hg194596
hg184596
hg174596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695488
Samples
Known GenesLINC00371
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518074
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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