A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790632



Internal ID21235970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129889648..129889648hg38UCSC Ensembl
chr11:129759543..129759543hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696635
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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