A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366522



Internal ID21024075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158820374..158911306hg38UCSC Ensembl
chr3:158538163..158629095hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3890933
hg1990933
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094647
Samples
Known GenesMFSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366522
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