A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv807737



Internal ID16101693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:36062873..36065921hg38UCSC Ensembl
Innerchr13:36637010..36640058hg19UCSC Ensembl
Innerchr13:35535010..35538058hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383049
hg193049
hg183049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561490
Supporting Variants
Samples
Known GenesDCLK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv807737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer