A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052984



Internal ID21962218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46443394..46443394hg38UCSC Ensembl
chr1:46909066..46909066hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520720
Samples
Known GenesLOC729041
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052984
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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