A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569299



Internal ID16010022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44306444..44483877hg38UCSC Ensembl
Innerchr15:44598642..44776075hg19UCSC Ensembl
Innerchr15:42385934..42563367hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38177434
hg19177434
hg18177434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4510n54
Supporting Variantsnssv842442
Samples
Known GenesCASC4, CTDSPL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569299
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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