A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066540



Internal ID21457598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86521870..86521870hg38UCSC Ensembl
chr1:86987553..86987553hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608114
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066540
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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