A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147013



Internal ID346219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22673382..22682625hg38UCSC Ensembl
chr14:23142591..23151834hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389244
hg199244
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147013
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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