A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155179



Internal ID22085684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52095388..52259703hg38UCSC Ensembl
Outerchr15:52089192..52263592hg38UCSC Ensembl
Innerchr15:52387585..52551900hg19UCSC Ensembl
Outerchr15:52381389..52555789hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38174401
hg19174401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011086
Samples
Known GenesBCL2L10, GNB5, LOC100129973, MYO5C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155179
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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