A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162657



Internal ID21460340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72198383..72198383hg38UCSC Ensembl
chr9:74813299..74813299hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642703
Supporting Variants
SamplesHG02818
Known GenesGDA
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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