A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052434



Internal ID19141653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85135020..85268380hg38UCSC Ensembl
Innerchr15:85678251..85811611hg19UCSC Ensembl
Innerchr15:83479255..83612615hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38133361
hg19133361
hg18133361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555064
Samples
Known GenesLOC440300, LOC642423, PDE8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052434
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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