A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145972



Internal ID21466834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73973430..73973430hg38UCSC Ensembl
chr8:74885665..74885665hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg382794
hg192794
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625450
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145972
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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