A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057248



Internal ID21966481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59025189..59025189hg38UCSC Ensembl
chr1:59490861..59490861hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38923
hg19923
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057248
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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