A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575699



Internal ID20948770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2283957..2288161hg38UCSC Ensembl
chr11:2305187..2309391hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384205
hg194205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575699
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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