A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618526



Internal ID20991597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121678401..121690100hg38UCSC Ensembl
chr6:121999547..122011246hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3811700
hg1911700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618526
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