A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589368



Internal ID20962439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6523416..6524595hg38UCSC Ensembl
chr12:6632582..6633761hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381180
hg191180
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226750
Samples
Known GenesNCAPD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589368
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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