A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059693



Internal ID21968926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2875326..2875407hg38UCSC Ensembl
chr19:2875324..2875405hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635875
Samples
Known GenesZNF556
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059693
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