A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041333



Internal ID21950668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162466195..162466195hg38UCSC Ensembl
chr1:162435985..162435985hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041333
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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