A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151395



Internal ID21423919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117610806..117610806hg38UCSC Ensembl
chr8:118623045..118623045hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639501
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151395
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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