A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4012182



Internal ID22073813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93187828..93217551hg38UCSC Ensembl
Outerchr15:93184918..93222333hg38UCSC Ensembl
Innerchr15:93731057..93760780hg19UCSC Ensembl
Outerchr15:93728147..93765562hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3837416
hg1937416
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155207
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4012182
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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