A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790036



Internal ID21235374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46722034..46722034hg38UCSC Ensembl
chr11:46743584..46743584hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13677934
Samples
Known GenesF2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790036
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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