A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456008



Internal ID21113561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32928988..33070525hg38UCSC Ensembl
chr11:32950534..33092071hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38141538
hg19141538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1017n223
Supporting Variantsnssv18193784
Samples
Known GenesDEPDC7, QSER1, TCP11L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456008
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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