A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351380



Internal ID21008933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42928033..42988319hg38UCSC Ensembl
chr2:43155173..43215459hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3860287
hg1960287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351380
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