A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266292



Internal ID20475510
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 StatusS
Merged Variantsnsv4745747
Supporting Variants
Samples
Known GenesADAM20P1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266292
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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