A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571026



Internal ID20944097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106514089..106536339hg38UCSC Ensembl
chr4:107435246..107457496hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3822251
hg1922251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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