A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952619



Internal ID16954806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45636003..45647302hg38UCSC Ensembl
Outerchr15:45928201..45939500hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3811300
hg1911300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999086
SamplesBILGI_BIOE
Known GenesSQRDL
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952619
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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