A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356796



Internal ID21014349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:80349921..81012219hg38UCSC Ensembl
chr3:80399071..81061370hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg38662299
hg19662300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4930n223
Supporting Variantsnssv18210037
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer