A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179470



Internal ID20746510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19819642..19881774hg38UCSC Ensembl
chr13:20393782..20455914hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3862133
hg1962133
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490113
Supporting Variants
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179470
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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