A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578481



Internal ID20951552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71774183..71775815hg38UCSC Ensembl
chr12:72167963..72169595hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381633
hg191633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227900
Samples
Known GenesRAB21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578481
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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