A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4008192



Internal ID22069823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70841566..70859367hg38UCSC Ensembl
Outerchr13:70834325..70862174hg38UCSC Ensembl
Innerchr13:71415698..71433499hg19UCSC Ensembl
Outerchr13:71408457..71436306hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3827850
hg1927850
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154936
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4008192
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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