A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049314



Internal ID21958547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63053819..63053819hg38UCSC Ensembl
chr1:63519490..63519490hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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