A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790429



Internal ID21235767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703069..56703069hg38UCSC Ensembl
chr11:56470545..56470545hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811069
hg1911069
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13696963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790429
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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