A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525868



Internal ID15453161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84921267..84956998hg38UCSC Ensembl
Innerchr15:85464498..85500229hg19UCSC Ensembl
Innerchr15:83265502..83301233hg18UCSC Ensembl
Innerchr15:83265502..83301233hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3835732
hg1935732
hg1835732
hg1735732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702068
Samples
Known GenesSLC28A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525868
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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