A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569366



Internal ID20942437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118281033..118281149hg38UCSC Ensembl
chr8:119293272..119293388hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277056
Samples
Known GenesSAMD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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