A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589524



Internal ID21781567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16260586..16260586hg38UCSC Ensembl
chr10:16302585..16302585hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085983
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589524
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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