A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145453



Internal ID344658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:52810805..52846065hg38UCSC Ensembl
chr14:53277523..53312783hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3835261
hg1935261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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