A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689306



Internal ID112972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:77025074..77025083hg38UCSC Ensembl
chr12:77418854..77418863hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542104
Supporting Variants
Samples
Known GenesE2F7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689306
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011418


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