A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582198



Internal ID21774241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:30059604..30059604hg38UCSC Ensembl
chr10:30348533..30348533hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582198
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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