A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357923



Internal ID21015476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183252901..183254800hg38UCSC Ensembl
chr3:182970689..182972588hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098483
Samples
Known GenesB3GNT5, MCF2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357923
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