A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569428



Internal ID16356837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52777677..52847848hg38UCSC Ensembl
Innerchr15:53069874..53140045hg19UCSC Ensembl
Innerchr15:50857166..50927337hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3870172
hg1970172
hg1870172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843015
Samples
Known GenesONECUT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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