A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578053



Internal ID20951124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45028722..45029726hg38UCSC Ensembl
chr11:45050273..45051277hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578053
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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