A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732606



Internal ID20508530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168538960..168539272hg38UCSC Ensembl
chr2:169395470..169395782hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289773
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732606
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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