A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494929



Internal ID272057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45956758..46229186hg38UCSC Ensembl
chr14:46425961..46698389hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38272429
hg19272429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694674
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494929
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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