A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578196



Internal ID20951267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:99191931..99194000hg38UCSC Ensembl
chr12:99585709..99587778hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382070
hg192070
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223905
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578196
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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