A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088691



Internal ID21464786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66971228..66971228hg38UCSC Ensembl
chr17:64967344..64967344hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662011
Supporting Variants
SamplesHG03065
Known GenesCACNG4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088691
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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