A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592283



Internal ID20965354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56666926..56668080hg38UCSC Ensembl
chr12:57060710..57061864hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231154
Samples
Known GenesPTGES3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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