A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578773



Internal ID20951844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31374229..31374486hg38UCSC Ensembl
chr16:31385550..31385807hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243527
Samples
Known GenesITGAX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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