A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033639



Internal ID90116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21057581..21057636hg38UCSC Ensembl
chr10:21346510..21346565hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142081
Supporting Variants
Samples
Known GenesNEBL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033639
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.30408


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