A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585582



Internal ID21777625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:129145689..129145689hg38UCSC Ensembl
chr8:130157935..130157935hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585582
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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