A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577898



Internal ID20950969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:876350..877228hg38UCSC Ensembl
chr12:985516..986394hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228691
Samples
Known GenesWNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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