A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152460



Internal ID21424377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102631763..102631763hg38UCSC Ensembl
chr8:103643991..103643991hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640624
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152460
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer