A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581637



Internal ID20954708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:127916806..127917559hg38UCSC Ensembl
chr12:128401351..128402104hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231826
Samples
Known GenesLINC00507
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581637
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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