A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580222



Internal ID20953293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53395952..53397481hg38UCSC Ensembl
chr12:53789736..53791265hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226292
Samples
Known GenesSP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580222
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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