A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472173



Internal ID21129726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32963193..33107112hg38UCSC Ensembl
chr11:32984739..33128658hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38143920
hg19143920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1017n223
Supporting Variantsnssv18177809
Samples
Known GenesCSTF3, DEPDC7, LINC00294, QSER1, TCP11L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472173
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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