A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569506



Internal ID16356915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54423352..54504394hg38UCSC Ensembl
Innerchr15:54715550..54796592hg19UCSC Ensembl
Innerchr15:52502842..52583884hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3881043
hg1981043
hg1881043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4541n54
Supporting Variantsnssv1148875, nssv843296
SamplesHGDP00592
Known GenesUNC13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569506
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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