A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413421



Internal ID21070974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64936991..64947695hg38UCSC Ensembl
chr5:64232818..64243522hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3810705
hg1910705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214098
Samples
Known GenesCWC27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413421
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