A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575931



Internal ID20949002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120633527..120634154hg38UCSC Ensembl
chr12:121071330..121071957hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575931
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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