A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066498



Internal ID21473594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84737661..84737661hg38UCSC Ensembl
chr1:85203344..85203344hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614300
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066498
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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