A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355968



Internal ID21013521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132811040..132821970hg38UCSC Ensembl
chr3:132529884..132540814hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3810931
hg1910931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208977
Samples
Known GenesNPHP3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355968
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