A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906066



Internal ID22681260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7917707..7918782hg38UCSC Ensembl
chr4:7919434..7920509hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425458
Samples
Known GenesAFAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906066
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