A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418213



Internal ID22476083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87073922..87074011hg38UCSC Ensembl
chr5:86369739..86369828hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906499
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418213
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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