A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17453008



Internal ID22510881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150811445..150814475hg38UCSC Ensembl
chr1:150783921..150786951hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828347
Supporting Variants
Samples
Known GenesARNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17453008
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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