A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493191



Internal ID22551120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50077852..50081795hg38UCSC Ensembl
chr3:50115285..50119228hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383944
hg193944
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836362
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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