A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154345



Internal ID22084850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:172958601..173164518hg38UCSC Ensembl
Outerchr1:172953785..173169742hg38UCSC Ensembl
Innerchr1:172927741..173133657hg19UCSC Ensembl
Outerchr1:172922925..173138881hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38215958
hg19215957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv21n97
Supporting Variantsnssv4005173
Samples
Known GenesTNFSF18
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154345
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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