A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580112



Internal ID20953183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8839944..8840174hg38UCSC Ensembl
chr12:8992540..8992770hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228726
Samples
Known GenesA2ML1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580112
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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