A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796418



Internal ID21241756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88461046..88461099hg38UCSC Ensembl
chr16:88527454..88527507hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685626
Samples
Known GenesZFPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796418
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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