A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586520



Internal ID20959591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10187722..10188093hg38UCSC Ensembl
chr12:10340321..10340692hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223492
Samples
Known GenesTMEM52B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586520
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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