A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704166



Internal ID127832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90022066..90034066hg38UCSC Ensembl
chr15:90565298..90577298hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812001
hg1912001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522824
Supporting Variants
Samples
Known GenesZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704166
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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