A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582006



Internal ID20955077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108095884..108096895hg38UCSC Ensembl
chr11:107966611..107967622hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231693
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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