A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366033



Internal ID21023586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3962495..4177076hg38UCSC Ensembl
chr3:4004179..4218760hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38214582
hg19214582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4764n223
Supporting Variantsnssv18100890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366033
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