A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734417



Internal ID20510352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85273981..85274069hg38UCSC Ensembl
chr8:86186210..86186298hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275558
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734417
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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