A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060007



Internal ID21969241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9819398..9820571hg38UCSC Ensembl
chr19:9930074..9931247hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381174
hg191174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060007
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