A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474632



Internal ID21132185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118992590..119006093hg38UCSC Ensembl
chr11:118863300..118876803hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3813504
hg1913504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196207
Samples
Known GenesCCDC84, RPL23AP64
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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