A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892432



Internal ID22667482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153369644..153372436hg38UCSC Ensembl
chr4:154290796..154293588hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382793
hg192793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411681
Samples
Known GenesMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892432
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