A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611921



Internal ID21803968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22676205..22679802hg38UCSC Ensembl
chr14:23145414..23149011hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383598
hg193598
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611921
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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