A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892455



Internal ID22667506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:97368692..97369493hg38UCSC Ensembl
chr5:96704396..96705197hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892455
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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