A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978991



Internal ID53369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11022854..11022905hg38UCSC Ensembl
chr6:11023087..11023138hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412107
Supporting Variants
Samples
Known GenesELOVL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978991
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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