A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104718



Internal ID21270648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:219827276..219928640hg38UCSC Ensembl
Innerchr2:220691997..220793361hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38101365
hg19101365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118162
Supporting Variants
Samplessample153
Known GenesMIR4268
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104718
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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