A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892571



Internal ID22667624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117046754..117052150hg38UCSC Ensembl
chr5:116382450..116387846hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg385397
hg195397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1708n209
Supporting Variantsnssv17420975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892571
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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