A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219789



Internal ID20786829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101605715..101606607hg38UCSC Ensembl
chr12:101999493..102000385hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588942
Supporting Variants
Samples
Known GenesMYBPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219789
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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