A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464208



Internal ID22522093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231307233..231308766hg38UCSC Ensembl
chr1:231442979..231444512hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464208
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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