A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607252



Internal ID21799299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93981936..93981936hg38UCSC Ensembl
chr14:94448282..94448282hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607252
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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