A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056105



Internal ID21965338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27710990..27710990hg38UCSC Ensembl
chr2:27933857..27933857hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056105
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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