A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580488



Internal ID20953559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62610971..62611500hg38UCSC Ensembl
chr12:63004751..63005280hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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