A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451279



Internal ID22509151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121712192..121717070hg38UCSC Ensembl
chr10:123471706..123476584hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384879
hg194879
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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