A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162546



Internal ID21403732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87746557..87746557hg38UCSC Ensembl
chr9:90361472..90361472hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632427
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162546
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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