A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006922



Internal ID20573962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105473664..105474231hg38UCSC Ensembl
chr13:106126013..106126580hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491021
Supporting Variants
Samples
Known GenesDAOA, DAOA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006922
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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