A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557959



Internal ID21882314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29407553..29407553hg38UCSC Ensembl
chr8:29265070..29265070hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557959
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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