A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411066



Internal ID22468936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135412497..135412552hg38UCSC Ensembl
chr5:134748187..134748242hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411066
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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