A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590805



Internal ID20963876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22057826..22058502hg38UCSC Ensembl
chr12:22210760..22211436hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231479
Samples
Known GenesCMAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590805
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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