A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691788



Internal ID115454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74552388..74592187hg38UCSC Ensembl
chr13:75126525..75166324hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3839800
hg1939800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510960
Supporting Variants
Samples
Known GenesLINC00347
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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