A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343732



Internal ID21001285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183093782..183098128hg38UCSC Ensembl
chr2:183958510..183962856hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg384347
hg194347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081647
Samples
Known GenesDUSP19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343732
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