A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565533



Internal ID20938604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13198995..13199080hg38UCSC Ensembl
chr8:13056504..13056589hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277135
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565533
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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