A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587068



Internal ID20960139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47781995..47782795hg38UCSC Ensembl
chr11:47803547..47804347hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224675
Samples
Known GenesNUP160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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