A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418509



Internal ID22476379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86573590..86574921hg38UCSC Ensembl
chr3:86622740..86624071hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5907378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418509
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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