A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006394



Internal ID20573434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102731634..102732272hg38UCSC Ensembl
chr13:103383984..103384622hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490854
Supporting Variants
Samples
Known GenesCCDC168
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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