A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405558



Internal ID21063111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55281374..55293733hg38UCSC Ensembl
chr6:55146172..55158531hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3812360
hg1912360
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219147
Samples
Known GenesHCRTR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405558
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