A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412429



Internal ID21069982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53757615..53763688hg38UCSC Ensembl
chr5:53053445..53059518hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg386074
hg196074
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412429
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