A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356877



Internal ID21014430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50800016..50806605hg38UCSC Ensembl
chr3:50837447..50844036hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg386590
hg196590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102236
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356877
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