A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952009



Internal ID17300883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:81293460..81298559hg38UCSC Ensembl
Outerchr15:81585801..81590900hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999152
SamplesBILGI_BIOE
Known GenesIL16
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952009
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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