A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049446



Internal ID21958679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220466561..220466561hg38UCSC Ensembl
chr1:220639903..220639903hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049446
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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