A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518260



Internal ID21842619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10059..10059hg38UCSC Ensembl
chr1:10059..10059hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383242
hg193242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042599
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518260
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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