A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225550



Internal ID20792590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45968681..45969944hg38UCSC Ensembl
chr12:46362464..46363727hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593781
Supporting Variants
Samples
Known GenesSCAF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225550
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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