A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594741



Internal ID20967812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42340308..42341059hg38UCSC Ensembl
chr12:42734110..42734861hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226965
Samples
Known GenesPPHLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594741
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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