A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046030



Internal ID21955282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202099623..202099623hg38UCSC Ensembl
chr2:202964346..202964346hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535083
Samples
Known GenesLOC100652824
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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