A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587650



Internal ID20960721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118071393..118075429hg38UCSC Ensembl
chr12:118509198..118513234hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg384037
hg194037
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219505
Samples
Known GenesVSIG10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587650
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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