A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144476



Internal ID21465773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64686201..64686201hg38UCSC Ensembl
chr8:65598758..65598758hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625953
Supporting Variants
SamplesHG03065
Known GenesCYP7B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144476
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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