A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696936



Internal ID120602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37507703..37551158hg38UCSC Ensembl
chr14:37976908..38020363hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3843456
hg1943456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505025
Supporting Variants
Samples
Known GenesMIPOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696936
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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