A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409624



Internal ID21067177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:84460887..84491582hg38UCSC Ensembl
chr5:83756705..83787400hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3830696
hg1930696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409624
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