A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143516



Internal ID20710556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54905401..54908600hg38UCSC Ensembl
chr6:54770199..54773398hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407328
Supporting Variants
Samples
Known GenesFAM83B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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