A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951439



Internal ID17300313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:65943166..65955265hg38UCSC Ensembl
Outerchr8:66855401..66867500hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999292
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951439
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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