A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738238



Internal ID20514206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69276762..69290045hg38UCSC Ensembl
chr2:69503894..69517177hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3813284
hg1913284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738238
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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