A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17629386



Internal ID21821433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7644004..7644004hg38UCSC Ensembl
chr19:7708890..7708890hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102080
Supporting Variants
Samples
Known GenesSTXBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17629386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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