A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359341



Internal ID21016894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46721861..46744356hg38UCSC Ensembl
chr3:46763351..46785846hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3822496
hg1922496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209285
Samples
Known GenesPRSS45, PRSS46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359341
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