A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237752



Internal ID20804792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53118602..53317689hg38UCSC Ensembl
chr14:53585320..53784407hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38199088
hg19199088
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576130
Supporting Variants
Samples
Known GenesDDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237752
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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