A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695201



Internal ID118867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45743365..46201879hg38UCSC Ensembl
chr14:46212568..46671082hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38458515
hg19458515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499386
Supporting Variants
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695201
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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