A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584586



Internal ID20957657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66161967..66171468hg38UCSC Ensembl
chr12:66555747..66565248hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg389502
hg199502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227365
Samples
Known GenesTMBIM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584586
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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