A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587985



Internal ID20961056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33029501..33029985hg38UCSC Ensembl
chr11:33051047..33051531hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1019n223
Supporting Variantsnssv18219966
Samples
Known GenesDEPDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587985
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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