A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558631



Internal ID20931702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100188352..100189305hg38UCSC Ensembl
chr8:101200580..101201533hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38954
hg19954
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7437n223
Supporting Variantsnssv18275881
Samples
Known GenesSPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558631
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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