A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966895



Internal ID22741830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116434944..116434944hg38UCSC Ensembl
chr5:115770640..115770640hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966895
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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