A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584121



Internal ID20957192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68152893..68155036hg38UCSC Ensembl
chr10:69912650..69914793hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233575
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584121
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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