A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406071



Internal ID21063624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54947901..55002700hg38UCSC Ensembl
chr6:54812699..54867498hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3854800
hg1954800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6188n223
Supporting Variantsnssv18218152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406071
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