A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894790



Internal ID22669865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81158352..81172108hg38UCSC Ensembl
chr5:80454171..80467927hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3813757
hg1913757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425064
Samples
Known GenesRASGRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894790
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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