A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17102334



Internal ID21454331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77820943..77820943hg38UCSC Ensembl
chr18:75532899..75532899hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652673
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17102334
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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