A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369121



Internal ID21026674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11840264..11879924hg38UCSC Ensembl
chr3:11881738..11921398hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3839661
hg1939661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207891
Samples
Known GenesTAMM41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369121
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