A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732327



Internal ID20508251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70825317..70825396hg38UCSC Ensembl
chr14:71292034..71292113hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732327
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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