A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923679



Internal ID22698906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85280649..85296123hg38UCSC Ensembl
chr8:86192878..86208352hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3815475
hg1915475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435560
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923679
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