A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584090



Internal ID20957161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118877448..118878495hg38UCSC Ensembl
chr12:119315253..119316300hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381048
hg191048
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584090
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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