A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17612651



Internal ID21804698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91521418..91521418hg38UCSC Ensembl
chr14:91987762..91987762hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6085862
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17612651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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