A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888513



Internal ID22663520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45399953..45400068hg38UCSC Ensembl
chr4:45401970..45402085hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888513
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