A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579153



Internal ID20952224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68212259..68212621hg38UCSC Ensembl
chr12:68606039..68606401hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231120
Samples
Known GenesIL26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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