A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366966



Internal ID21024519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183252901..183253300hg38UCSC Ensembl
chr3:182970689..182971088hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098482
Samples
Known GenesB3GNT5, MCF2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366966
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer