A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599762



Internal ID21791809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73304951..73305027hg38UCSC Ensembl
chr14:73771659..73771735hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035753
Supporting Variants
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599762
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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