A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955329



Internal ID17304202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:118475454..118484753hg38UCSC Ensembl
Outerchr3:118194301..118203600hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg389300
hg199300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001446
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955329
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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