A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578701



Internal ID20951772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32887539..32888135hg38UCSC Ensembl
chr12:33040473..33041069hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226093
Samples
Known GenesPKP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578701
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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