A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592143



Internal ID21784186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119684572..119684572hg38UCSC Ensembl
chr10:121444084..121444084hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592143
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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