A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354466



Internal ID21012019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63859559..63872290hg38UCSC Ensembl
chr2:64086693..64099424hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3812732
hg1912732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089266
Samples
Known GenesUGP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354466
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