A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533952



Internal ID20907313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30950770..30983660hg38UCSC Ensembl
chr19:31441676..31474566hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3832891
hg1932891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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