A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499865



Internal ID276819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105008665..105008959hg38UCSC Ensembl
chr14:105475002..105475296hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499865
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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