A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466441



Internal ID22524332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:192896758..192926607hg38UCSC Ensembl
chr1:192865888..192895737hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg3829850
hg1929850
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5828807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466441
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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