A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162958



Internal ID21456281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90716628..90716628hg38UCSC Ensembl
chr9:93478910..93478910hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381169
hg191169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636939
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162958
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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