A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359403



Internal ID21016956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75275001..75520300hg38UCSC Ensembl
chr3:75324152..75569451hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38245300
hg19245300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4912n223
Supporting Variantsnssv18208730
Samples
Known GenesFAM86DP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359403
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