A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568534



Internal ID16355943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24847119..24874807hg38UCSC Ensembl
Innerchr15:25092266..25119954hg19UCSC Ensembl
Innerchr15:22643359..22671047hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3827689
hg1927689
hg1827689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838768
Samples
Known GenesSNRPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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