A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983035



Internal ID21892378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23897126..23897711hg38UCSC Ensembl
chr1:24223616..24224201hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518576
Samples
Known GenesCNR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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