A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044125



Internal ID18786656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24984759..25041425hg38UCSC Ensembl
Innerchr15:25229906..25286572hg19UCSC Ensembl
Innerchr15:22780999..22837665hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3856667
hg1956667
hg1856667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545397
Samples
Known GenesPWAR5, SNORD108, SNORD64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044125
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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