A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413567



Internal ID22471437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87038746..87057733hg38UCSC Ensembl
chr5:86334563..86353550hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3818988
hg1918988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5894678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413567
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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