A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467643



Internal ID21125196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73469801..73483900hg38UCSC Ensembl
chr11:73180846..73194945hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192564
Samples
Known GenesFAM168A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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