A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575539



Internal ID20948610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125008101..125009809hg38UCSC Ensembl
chr8:126020343..126022051hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381709
hg191709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276169
Samples
Known GenesSQLE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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