A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508308



Internal ID285003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21203636..21204510hg38UCSC Ensembl
chr14:21671795..21672669hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693843
Samples
Known GenesLINC00641
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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