A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699252



Internal ID122918
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 StatusS
Merged Variantsnsv5513688
Supporting Variants
Samples
Known GenesZNF410
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699252
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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