A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594140



Internal ID20967211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53393620..53394099hg38UCSC Ensembl
chr12:53787404..53787883hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221590
Samples
Known GenesSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594140
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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