A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526298



Internal ID20899659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22901232..23494651hg38UCSC Ensembl
chr19:23084034..23677453hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38593420
hg19593420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198515
Samples
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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