A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030995



Internal ID88364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1548030..1548061hg38UCSC Ensembl
chr10:1590225..1590256hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545688
Supporting Variants
Samples
Known GenesADARB2, ADARB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030995
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002966


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