A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585044



Internal ID20958115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83175297..83175685hg38UCSC Ensembl
chr11:82886339..82886727hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230082
Samples
Known GenesPCF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585044
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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