A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050521



Internal ID18793052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:38303495..38336196hg38UCSC Ensembl
Innerchr15:38595696..38628397hg19UCSC Ensembl
Innerchr15:36382988..36415689hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3832702
hg1932702
hg1832702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552239
Samples
Known GenesSPRED1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050521
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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