A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572746



Internal ID20945817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13191240..13192006hg38UCSC Ensembl
chr8:13048749..13049515hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277134
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572746
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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