A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576254



Internal ID20949325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122969370..122970181hg38UCSC Ensembl
chr11:122840078..122840889hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576254
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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