A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576716



Internal ID20949787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50406844..50407735hg38UCSC Ensembl
chr12:50800627..50801518hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38892
hg19892
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230477
Samples
Known GenesLARP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576716
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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