A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464978



Internal ID22522866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:194258849..194270839hg38UCSC Ensembl
chr1:194227979..194239969hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3811991
hg1911991
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5829126
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464978
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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