A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17425257



Internal ID22483127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156585939..156590291hg38UCSC Ensembl
chr3:156303728..156308080hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17425257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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