A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264220



Internal ID20831260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158500774..158878862hg38UCSC Ensembl
chr4:159421926..159800014hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38378089
hg19378089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565615
Supporting Variants
Samples
Known GenesC4orf46, ETFDH, FNIP2, PPID, RXFP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264220
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00133


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