A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544490



Internal ID20917728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45805801..45808600hg38UCSC Ensembl
chr20:44434440..44437239hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202898
Samples
Known GenesDNTTIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544490
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