A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699249



Internal ID122915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73888038..73888089hg38UCSC Ensembl
chr14:74354741..74354792hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430751
Supporting Variants
Samples
Known GenesZNF410
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699249
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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