A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2791084



Internal ID21236422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64270856..64270932hg38UCSC Ensembl
chr11:64038328..64038404hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13681872
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2791084
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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