A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17632645



Internal ID21824692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32306195..32306195hg38UCSC Ensembl
chr19:32797101..32797101hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108262
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17632645
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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