A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502955



Internal ID279804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70637368..70639562hg38UCSC Ensembl
chr14:71104085..71106279hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382195
hg192195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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