A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513688



Internal ID290204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73918638..73919894hg38UCSC Ensembl
chr14:74385341..74386597hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381257
hg191257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699252
Samples
Known GenesZNF410
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513688
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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