A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952626



Internal ID16954813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:51833004..51848203hg38UCSC Ensembl
Outerchr15:52125201..52140400hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3815200
hg1915200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999093
SamplesBILGI_BIOE
Known GenesTMOD3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952626
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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