A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18012570



Internal ID20579610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73417651..75973295hg38UCSC Ensembl
chr13:73991788..76547431hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg382555645
hg192555644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492903
Supporting Variants
Samples
Known GenesC13orf45, COMMD6, CTAGE11P, KLF12, LINC00347, LINC00381, LMO7, TBC1D4, UCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18012570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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