A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587091



Internal ID20960162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:22653153..22653387hg38UCSC Ensembl
chr12:22806087..22806321hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229169
Samples
Known GenesETNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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