A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950365



Internal ID16952552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:101169344..101345943hg38UCSC Ensembl
Outerchr4:102090501..102267100hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38176600
hg19176600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996753
SamplesBILGI_BIOE
Known GenesMIR8066, PPP3CA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950365
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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