A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155208



Internal ID22085713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93187828..93222333hg38UCSC Ensembl
Outerchr15:93184918..93224692hg38UCSC Ensembl
Innerchr15:93731057..93765562hg19UCSC Ensembl
Outerchr15:93728147..93767921hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3839775
hg1939775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv101n97
Supporting Variantsnssv4012184, nssv4012183
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155208
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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