A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790601



Internal ID21235939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:115599410..115599410hg38UCSC Ensembl
chr11:115470128..115470128hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790601
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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