A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340072



Internal ID20997625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202967181..202991875hg38UCSC Ensembl
chr2:203831904..203856598hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg3824695
hg1924695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208068
Samples
Known GenesCARF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340072
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