A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373497



Internal ID21031050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164915701..165128400hg38UCSC Ensembl
chr3:164633489..164846188hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38212700
hg19212700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208632
Samples
Known GenesSI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373497
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