A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17592306



Internal ID21784349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8985436..8985436hg38UCSC Ensembl
chr10:9027399..9027399hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17592306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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