A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054877



Internal ID21964110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220844370..220844370hg38UCSC Ensembl
chr1:221017712..221017712hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054877
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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