A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582777



Internal ID20955848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126248012..126248388hg38UCSC Ensembl
chr11:126117907..126118283hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227227
Samples
Known GenesFAM118B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582777
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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