A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583068



Internal ID20956139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43079008..43081273hg38UCSC Ensembl
chr10:43574456..43576721hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382266
hg192266
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225648
Samples
Known GenesRET
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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