A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569539



Internal ID16010262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55430015..55963576hg38UCSC Ensembl
Innerchr15:55722213..56255774hg19UCSC Ensembl
Innerchr15:53509505..54043066hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38533562
hg19533562
hg18533562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843416
Samples
Known GenesDYX1C1, DYX1C1-CCPG1, NEDD4, PRTG, PYGO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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