A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096556



Internal ID21284357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72834646..72836414hg38UCSC Ensembl
Innerchr16:72868545..72870313hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381769
hg191769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113213
Supporting Variants
Samplessample360
Known GenesZFHX3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096556
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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