A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577967



Internal ID20951038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56683525..56685570hg38UCSC Ensembl
chr12:57077309..57079354hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382046
hg192046
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229343
Samples
Known GenesPTGES3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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