A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579395



Internal ID20952466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77825714..77826358hg38UCSC Ensembl
chr11:77536760..77537404hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1233n223
Supporting Variantsnssv18235235
Samples
Known GenesAAMDC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579395
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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