A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586591



Internal ID20959662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50172221..50172842hg38UCSC Ensembl
chr12:50566004..50566625hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586591
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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