A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589608



Internal ID20962679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70402651..70403328hg38UCSC Ensembl
chr12:70796431..70797108hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221354
Samples
Known GenesKCNMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589608
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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