A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232940



Internal ID20799980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6659813..6661270hg38UCSC Ensembl
chr12:6768979..6770436hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588927
Supporting Variants
Samples
Known GenesING4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232940
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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