A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579515



Internal ID20952586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60067849..60068548hg38UCSC Ensembl
chr11:59835322..59836021hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1200n223
Supporting Variantsnssv18224208
Samples
Known GenesMS4A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579515
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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