A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581118



Internal ID20954189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14572824..14574149hg38UCSC Ensembl
chr12:14725758..14727083hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581118
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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