A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591139



Internal ID20964210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27173584..27174148hg38UCSC Ensembl
chr10:27462513..27463077hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv666n223
Supporting Variantsnssv18221415
Samples
Known GenesMASTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591139
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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