A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987097



Internal ID21896440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200927531..200927612hg38UCSC Ensembl
chr2:201792254..201792335hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526237
Samples
Known GenesORC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987097
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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