A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155177



Internal ID22085682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51831619..51909706hg38UCSC Ensembl
Outerchr15:51823404..51913827hg38UCSC Ensembl
Innerchr15:52123816..52201903hg19UCSC Ensembl
Outerchr15:52115601..52206024hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3890424
hg1990424
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011083
Samples
Known GenesTMOD3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155177
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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