A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634852



Internal ID21826899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8009355..8014194hg38UCSC Ensembl
chr19:8074239..8079078hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384840
hg194840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6052743
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634852
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer