A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17481190



Internal ID22539094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72984763..72992943hg38UCSC Ensembl
chr1:73450446..73458626hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg388181
hg198181
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17481190
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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