A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954481



Internal ID16956668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:47449111..47451910hg38UCSC Ensembl
Outerchr3:47490601..47493400hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv125n73
Supporting Variantsnssv3001377
SamplesBILGI_BIOE
Known GenesSCAP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954481
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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