A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591349



Internal ID21783392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121712148..121717089hg38UCSC Ensembl
chr10:123471662..123476603hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg384942
hg194942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011419
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591349
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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