A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899305



Internal ID22674434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88032843..88032989hg38UCSC Ensembl
chr5:87328660..87328806hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899305
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