A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952612



Internal ID17301486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:41298603..41307002hg38UCSC Ensembl
Outerchr15:41590801..41599200hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999079
SamplesBILGI_BIOE
Known GenesOIP5-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952612
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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