A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515877



Internal ID15096484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43509826..43525854hg38UCSC Ensembl
Innerchr15:43802024..43818052hg19UCSC Ensembl
Innerchr15:41589316..41605344hg18UCSC Ensembl
Innerchr15:41589316..41605344hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3816029
hg1916029
hg1816029
hg1716029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673893, nssv665119
Samples
Known GenesMAP1A, RNU6-28P, TP53BP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515877
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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