A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892600



Internal ID22667653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115654880..115654952hg38UCSC Ensembl
chr5:114990577..114990649hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428217
Samples
Known GenesLOC102467217
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892600
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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