A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347828



Internal ID21005381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66621764..66624371hg38UCSC Ensembl
chr2:66848896..66851503hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347828
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