A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904214



Internal ID22679390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161564247..161564729hg38UCSC Ensembl
chr5:160991253..160991735hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904214
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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