A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903632



Internal ID22678801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175563933..175564249hg38UCSC Ensembl
chr5:174990936..174991252hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903632
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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