A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163167



Internal ID21428981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96300300..96300637hg38UCSC Ensembl
chr9:99062582..99062919hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597362
Supporting Variants
SamplesHG00731
Known GenesHSD17B3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163167
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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