A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006734



Internal ID20573774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100149505..100151834hg38UCSC Ensembl
chr13:100801759..100804088hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382330
hg192330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494713
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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