A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120413



Internal ID21476953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126165020..126166118hg38UCSC Ensembl
chr5:125500713..125501811hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583385
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120413
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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