A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631619



Internal ID21823666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28888401..28888401hg38UCSC Ensembl
chr19:29379308..29379308hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111336
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631619
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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