A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594318



Internal ID20967389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105339636..105340439hg38UCSC Ensembl
chr12:105733414..105734217hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231718
Samples
Known GenesC12orf75
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594318
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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