A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591878



Internal ID20964949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119268568..119270177hg38UCSC Ensembl
chr12:119706373..119707982hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381610
hg191610
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591878
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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