A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581979



Internal ID20955050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12551378..12551986hg38UCSC Ensembl
chr12:12704312..12704920hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236386
Samples
Known GenesDUSP16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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