A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569408



Internal ID16356817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51574975..51653903hg38UCSC Ensembl
Innerchr15:51867172..51946100hg19UCSC Ensembl
Innerchr15:49654464..49733392hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3878929
hg1978929
hg1878929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv842982
Samples
Known GenesDMXL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569408
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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