A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740872



Internal ID20516849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:71753917..71753971hg38UCSC Ensembl
chr14:72220634..72220688hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740872
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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