A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700210



Internal ID123876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105865571..106775160hg38UCSC Ensembl
chr14:106331781..107183399hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38909590
hg19851619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145610
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700210
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.11536


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