A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737755



Internal ID20513718
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 StatusM
Merged Variants
Supporting Variantsnssv16290722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737755
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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