A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037703



Internal ID21947046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70477851..70477904hg38UCSC Ensembl
chr14:70944568..70944621hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610238
Samples
Known GenesADAM20P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037703
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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