A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734626



Internal ID20510564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35874663..35874719hg38UCSC Ensembl
chr14:36343869..36343925hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734626
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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