A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358149



Internal ID21015702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82282693..82283467hg38UCSC Ensembl
chr3:82331844..82332618hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358149
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