A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604532



Internal ID21796579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:28888096..28888096hg38UCSC Ensembl
chr14:29357302..29357302hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084044
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604532
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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