A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499386



Internal ID276360
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 StatusM
Merged Variants
Supporting Variantsnssv17695201
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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