A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179730



Internal ID20746770
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 StatusS
Merged Variantsnsv6469764
Supporting Variants
Samples
Known GenesPRDM10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179730
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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