A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581842



Internal ID20954913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64426701..64427235hg38UCSC Ensembl
chr12:64820481..64821015hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38535
hg19535
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236882
Samples
Known GenesXPOT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581842
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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