A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17617000



Internal ID21809047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34443197..34443360hg38UCSC Ensembl
chr14:34912403..34912566hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035799
Supporting Variants
Samples
Known GenesSPTSSA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17617000
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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