A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580308



Internal ID20953379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110065359..110066271hg38UCSC Ensembl
chr12:110503164..110504076hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219012
Samples
Known GenesC12orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580308
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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