A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591725



Internal ID20964796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46206278..46207021hg38UCSC Ensembl
chr11:46227829..46228572hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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