A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461847



Internal ID21119400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108529012..108762128hg38UCSC Ensembl
chr11:108399739..108632855hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38233117
hg19233117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180328
Samples
Known GenesDDX10, EXPH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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