A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569301



Internal ID16356710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44505377..44522770hg38UCSC Ensembl
Innerchr15:44797575..44814968hg19UCSC Ensembl
Innerchr15:42584867..42602260hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3817394
hg1917394
hg1817394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842444
Samples
Known GenesCTDSPL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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