A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577508



Internal ID20950579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106058221..106058578hg38UCSC Ensembl
chr11:105928948..105929305hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1302n223
Supporting Variantsnssv18233962
Samples
Known GenesKBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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