A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899295



Internal ID22674424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:46109548..46109870hg38UCSC Ensembl
chr6:46077285..46077607hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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