A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563254



Internal ID20936325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97664243..97664756hg38UCSC Ensembl
chr8:98676471..98676984hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279193
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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