A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354539



Internal ID21012092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139184028..139188740hg38UCSC Ensembl
chr2:139941598..139946310hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg384713
hg194713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354539
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