A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590485



Internal ID20963556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50499941..50501581hg38UCSC Ensembl
chr12:50893724..50895364hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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