A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402285



Internal ID21059838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74649722..74713048hg38UCSC Ensembl
chr6:75359438..75422764hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3863327
hg1963327
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402285
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