A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043442



Internal ID21952746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165480353..165480353hg38UCSC Ensembl
chr1:165449590..165449590hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522969
Samples
Known GenesLOC400794
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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