A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949987



Internal ID17298861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:132483854..132492453hg38UCSC Ensembl
Outerchr8:133496101..133504700hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999328
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949987
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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