A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954458



Internal ID16956645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:31535409..31660708hg38UCSC Ensembl
Outerchr3:31576901..31702200hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg38125300
hg19125300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001354
SamplesBILGI_BIOE
Known GenesSTT3B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954458
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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