A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349890



Internal ID21007443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113177553..113178893hg38UCSC Ensembl
chr2:113935130..113936470hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg381341
hg191341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075588
Samples
Known GenesPSD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349890
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