A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460521



Internal ID22518404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:52362206..52370857hg38UCSC Ensembl
chr10:54121966..54130617hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg388652
hg198652
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460521
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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