A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290722



Internal ID20499940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35884501..35884774hg38UCSC Ensembl
chr14:36353707..36353980hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737755
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290722
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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