A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589287



Internal ID20962358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75081989..75324890hg38UCSC Ensembl
chr10:76841747..77084648hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38242902
hg19242902
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231570
Samples
Known GenesCOMTD1, DUSP13, SAMD8, VDAC2, ZNF503-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589287
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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