A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592783



Internal ID20965854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76162088..76162717hg38UCSC Ensembl
chr12:76555868..76556497hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232723
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592783
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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