A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18011391



Internal ID20578431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67472735..67524891hg38UCSC Ensembl
chr13:68046867..68099023hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3852157
hg1952157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18011391
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0002


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