A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008308



Internal ID22069939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110021263..110022852hg38UCSC Ensembl
Outerchr13:110020621..110026428hg38UCSC Ensembl
Innerchr13:110673610..110675199hg19UCSC Ensembl
Outerchr13:110672968..110678775hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154973
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008308
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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