A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544750



Internal ID20917987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39744486..39758521hg38UCSC Ensembl
chr20:38373128..38387163hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3814036
hg1914036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544750
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