A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628108



Internal ID21820155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19697012..19702846hg38UCSC Ensembl
chr19:19807821..19813655hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054672
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628108
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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