A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580000



Internal ID20953071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40055658..40058900hg38UCSC Ensembl
chr11:40077208..40080450hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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