A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577755



Internal ID20950826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11895216..11895837hg38UCSC Ensembl
chr16:11989073..11989694hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239859
Samples
Known GenesGSPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577755
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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