A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17426060



Internal ID22483930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53278223..53281537hg38UCSC Ensembl
chr3:53312239..53315557hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg383315
hg193319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5897224
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17426060
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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