A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583509



Internal ID20956580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11585370..11586991hg38UCSC Ensembl
chr11:11606917..11608538hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218874
Samples
Known GenesGALNT18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583509
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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