A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745747



Internal ID20521757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:70477788..70477841hg38UCSC Ensembl
chr14:70944505..70944558hg19UCSC 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 Variantsnssv16266292
Samples
Known GenesADAM20P1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745747
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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