A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140789



Internal ID21504831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:73094101..73094976hg38UCSC Ensembl
chr5:72389928..72390803hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579524
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140789
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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