A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789965



Internal ID21235303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19860117..19860117hg38UCSC Ensembl
chr11:19881663..19881663hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682110, nssv13695286
Samples
Known GenesNAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789965
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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