A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597767



Internal ID21789810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73278844..73278924hg38UCSC Ensembl
chr14:73745552..73745632hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036664
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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