A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892579



Internal ID22667632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152782044..152782234hg38UCSC Ensembl
chr4:153703196..153703386hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421021
Samples
Known GenesARFIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892579
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