A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013614



Internal ID76749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64643038..64643090hg38UCSC Ensembl
chr8:65555595..65555647hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549261
Supporting Variants
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013614
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.054963


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