A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162667



Internal ID21485041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:73595590..73595590hg38UCSC Ensembl
chr9:76210506..76210506hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38819
hg19819
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637934
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162667
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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