A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581275



Internal ID20954346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120348806..120349209hg38UCSC Ensembl
chr12:120786609..120787012hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220140
Samples
Known GenesMSI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581275
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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