A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687742



Internal ID111408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51169983..51174588hg38UCSC Ensembl
chr13:51744119..51748724hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg384606
hg194606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512680
Supporting Variants
Samples
Known GenesLINC00371
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687742
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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