A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17591334



Internal ID21783377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123546461..123546461hg38UCSC Ensembl
chr8:124558701..124558701hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069620
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17591334
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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