A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234034



Internal ID20801075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49760119..49760288hg38UCSC Ensembl
chr12:50153902..50154071hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595164
Supporting Variants
Samples
Known GenesTMBIM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234034
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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