A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561503



Internal ID20934574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69729385..69729526hg38UCSC Ensembl
chr8:70641620..70641761hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278585
Samples
Known GenesSLCO5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561503
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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