A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100390



Internal ID21511405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8432347..8432347hg38UCSC Ensembl
chr17:8335665..8335665hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659747
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100390
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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