A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461232



Internal ID22519115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80239921..80242406hg38UCSC Ensembl
chr10:81999677..82002162hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382486
hg192486
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461232
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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