A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573947



Internal ID20947018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33552666..35477570hg38UCSC Ensembl
chr4:33554288..35479192hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381924905
hg191924905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573947
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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