A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900556



Internal ID22675699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45431711..45591700hg38UCSC Ensembl
chr4:45433728..45593717hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38159990
hg19159990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900556
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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