A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047546



Internal ID21956780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708208..165708208hg38UCSC Ensembl
chr1:165677445..165677445hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534302
Samples
Known GenesLOC440700
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047546
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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