A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988634



Internal ID21897977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27320082..27320166hg38UCSC Ensembl
chr2:27542949..27543033hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519952
Samples
Known GenesMPV17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988634
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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