A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362988



Internal ID22588657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58944350..58946655hg38UCSC Ensembl
chr10:60704110..60706415hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362988
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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