A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730433



Internal ID20506345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160535696..160535835hg38UCSC Ensembl
chr2:161392207..161392346hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730433
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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