A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264863



Internal ID20831903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156898820..156899661hg38UCSC Ensembl
chr4:157819972..157820813hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38842
hg19842
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571899
Supporting Variants
Samples
Known GenesPDGFC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264863
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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