A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569429



Internal ID16356838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53008826..53037105hg38UCSC Ensembl
Innerchr15:53301023..53329302hg19UCSC Ensembl
Innerchr15:51088315..51116594hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3828280
hg1928280
hg1828280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843016
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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