A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237846



Internal ID20804886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56570916..56571711hg38UCSC Ensembl
chr14:57037634..57038429hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38796
hg19796
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592920
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237846
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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