A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537848



Internal ID20911180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16593534..16597413hg38UCSC Ensembl
chr21:17965854..17969733hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383880
hg193880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203791
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537848
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