A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410037



Internal ID21067590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:127921415..127950847hg38UCSC Ensembl
chr5:127257107..127286539hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3829433
hg1929433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215406
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410037
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