A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469764



Internal ID21127317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129899087..129916996hg38UCSC Ensembl
chr11:129768982..129786891hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3817910
hg1917910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179730
Samples
Known GenesPRDM10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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