A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340928



Internal ID20998481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21147301..21148700hg38UCSC Ensembl
chr2:21370173..21371572hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340928
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