A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555776



Internal ID20928847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90046984..91196055hg38UCSC Ensembl
chr8:91059212..92208283hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381149072
hg191149072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279003
Samples
Known GenesC8orf88, CALB1, DECR1, LINC00534, LINC01030, LRRC69, NECAB1, OTUD6B, TMEM55A, TMEM64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555776
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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