A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589912



Internal ID20962983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:20257230..20261724hg38UCSC Ensembl
chr12:20410164..20414658hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg384495
hg194495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228934
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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