A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587020



Internal ID20960091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121868769..121869333hg38UCSC Ensembl
chr12:122306675..122307239hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222813
Samples
Known GenesHPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587020
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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