A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584432



Internal ID20957503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14644260..14644883hg38UCSC Ensembl
chr12:14797194..14797817hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226513
Samples
Known GenesGUCY2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584432
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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