A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368639



Internal ID21026192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34525552..34525855hg38UCSC Ensembl
chr3:34567044..34567347hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368639
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