A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795836



Internal ID21241174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325361..69325428hg38UCSC Ensembl
chr16:69359264..69359331hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795836
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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