A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005172



Internal ID22066803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:172952732..173169742hg38UCSC Ensembl
Outerchr1:172946563..173172552hg38UCSC Ensembl
Innerchr1:172921872..173138881hg19UCSC Ensembl
Outerchr1:172915703..173141691hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38225990
hg19225989
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154340
Supporting Variants
Samples
Known GenesTNFSF18
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005172
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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