A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046733



Internal ID21955966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110310153..110310153hg38UCSC Ensembl
chr1:110852775..110852775hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530051
Samples
Known GenesLOC440600
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046733
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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