A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950478



Internal ID16952665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:87683683..87703282hg38UCSC Ensembl
Outerchr6:88393401..88413000hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3819600
hg1919600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997489
SamplesBILGI_BIOE
Known GenesAKIRIN2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950478
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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