A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155214



Internal ID22085719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:97274562..97290422hg38UCSC Ensembl
Outerchr15:97265179..97301760hg38UCSC Ensembl
Innerchr15:97817792..97833652hg19UCSC Ensembl
Outerchr15:97808409..97844990hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3836582
hg1936582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012195
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155214
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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