A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569583



Internal ID16356992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57351455..57483628hg38UCSC Ensembl
Innerchr15:57643653..57775826hg19UCSC Ensembl
Innerchr15:55430945..55563118hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38132174
hg19132174
hg18132174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4556n54
Supporting Variantsnssv843561, nssv843558, nssv843560, nssv843557, nssv843559
Samples
Known GenesCGNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569583
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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