A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896921



Internal ID22672018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3957769..3961362hg38UCSC Ensembl
chr6:3958003..3961596hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg383594
hg193594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896921
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