A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592360



Internal ID20965431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:99187925..99192353hg38UCSC Ensembl
chr12:99581703..99586131hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg384429
hg194429
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235354
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592360
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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