A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951973



Internal ID16954160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:63210802..63223801hg38UCSC Ensembl
Outerchr15:63503001..63516000hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999112
SamplesBILGI_BIOE
Known GenesRAB8B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951973
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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