A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561900



Internal ID20934971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93811912..93812735hg38UCSC Ensembl
chr8:94824140..94824963hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7423n223
Supporting Variantsnssv18279069
Samples
Known GenesTMEM67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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