A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521903



Internal ID15102510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32997748..33009307hg38UCSC Ensembl
Innerchr15:33289949..33301508hg19UCSC Ensembl
Innerchr15:31077241..31088800hg18UCSC Ensembl
Innerchr15:31077241..31088800hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3811560
hg1911560
hg1811560
hg1711560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694674
Samples
Known GenesFMN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521903
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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