A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413677



Internal ID22471547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73788159..73821864hg38UCSC Ensembl
chr3:73837310..73871015hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3833706
hg1933706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413677
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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