A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570060



Internal ID20943131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13213931..13215444hg38UCSC Ensembl
chr8:13071440..13072953hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277136
Samples
Known GenesDLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570060
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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