A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155199



Internal ID22085704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79704284..79727041hg38UCSC Ensembl
Outerchr15:79702285..79730764hg38UCSC Ensembl
Innerchr15:79996626..80019383hg19UCSC Ensembl
Outerchr15:79994627..80023106hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3828480
hg1928480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012130
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155199
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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