A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359592



Internal ID21017145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108247595..108250680hg38UCSC Ensembl
chr3:107966442..107969527hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383086
hg193086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359592
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