A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458054



Internal ID21115607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32991493..33036702hg38UCSC Ensembl
chr11:33013039..33058248hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3845210
hg1945210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989742
Samples
Known GenesDEPDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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