A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035232



Internal ID91224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71296899..71296903hg38UCSC Ensembl
chr10:73056656..73056660hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545714
Supporting Variants
Samples
Known GenesUNC5B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035232
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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