A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411123



Internal ID22468993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142793659..142793659hg38UCSC Ensembl
chr6:143114796..143114796hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967524
Supporting Variants
Samples
Known GenesHIVEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411123
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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