A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555803



Internal ID20928874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30235696..30236600hg38UCSC Ensembl
chr8:30093212..30094116hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277678
Samples
Known GenesMIR548O2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555803
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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