A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409897



Internal ID21067450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113013644..113030530hg38UCSC Ensembl
chr5:112349341..112366227hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3816887
hg1916887
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212434
Samples
Known GenesDCP2, MCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409897
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