A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790222



Internal ID21235560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31213134..31213134hg38UCSC Ensembl
chr11:31234681..31234681hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683548
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790222
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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