A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589314



Internal ID20962385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14749890..14750498hg38UCSC Ensembl
chr12:14902824..14903432hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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