A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561491



Internal ID16348900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36062873..36066278hg38UCSC Ensembl
Innerchr13:36637010..36640415hg19UCSC Ensembl
Innerchr13:35535010..35538415hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383406
hg193406
hg183406
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3118n54
Supporting Variantsnssv807739, nssv807741, nssv807738, nssv807740, nssv807742
Samples
Known GenesDCLK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561491
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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