A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752979



Internal ID20528839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27749226..27749226hg38UCSC Ensembl
chr2:27972093..27972093hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752979
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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