A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576989



Internal ID20950060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120780335..120781746hg38UCSC Ensembl
chr12:121218138..121219549hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381412
hg191412
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236086
Samples
Known GenesSPPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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