A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892289



Internal ID22667337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89369044..89369374hg38UCSC Ensembl
chr5:88664861..88665191hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892289
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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