A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161643



Internal ID21406235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34936995..34936995hg38UCSC Ensembl
chr9:34936992..34936992hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643396
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161643
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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