A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585443



Internal ID20958514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90123410..90191700hg38UCSC Ensembl
chr11:89856578..89924868hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3868291
hg1968291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231771
Samples
Known GenesNAALAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585443
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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