A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414455



Internal ID22472325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31657814..31658041hg38UCSC Ensembl
chr3:31699306..31699533hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414455
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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