A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578633



Internal ID20951704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67689843..67690244hg38UCSC Ensembl
chr12:68083623..68084024hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231340
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578633
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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