A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368283



Internal ID22593952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103956119..103961009hg38UCSC Ensembl
chr10:105715877..105720767hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg384891
hg194891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914422
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368283
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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