A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232772



Internal ID20799812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20764636..21233863hg38UCSC Ensembl
chr12:20917570..21386797hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38469228
hg19469228
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590452
Supporting Variants
Samples
Known GenesSLCO1B1, SLCO1B3, SLCO1B7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232772
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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