A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228481



Internal ID20795521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12174181..12175263hg38UCSC Ensembl
chr12:12327115..12328197hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg381083
hg191083
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581582
Supporting Variants
Samples
Known GenesLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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