A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045960



Internal ID21955212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128438382..128438382hg38UCSC Ensembl
chr2:129195956..129195956hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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