A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063532



Internal ID21433419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240060353..240060353hg38UCSC Ensembl
chr1:240223653..240223653hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618581
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063532
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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