A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472778



Internal ID21130331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62409196..62420436hg38UCSC Ensembl
chr11:62176668..62187908hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3811241
hg1911241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185229
Samples
Known GenesSCGB1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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