A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989017



Internal ID21898360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36505373..36505624hg38UCSC Ensembl
chr2:36732516..36732767hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527811
Samples
Known GenesCRIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989017
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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