A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556728



Internal ID20929799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26366549..26367140hg38UCSC Ensembl
chr4:26368171..26368762hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264978
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556728
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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