A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512571



Internal ID289122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27541423..27618215hg38UCSC Ensembl
chr14:28010629..28087421hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3876793
hg1976793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695805
Samples
Known GenesLINC00645
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512571
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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