A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950077



Internal ID17298951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:68252773..68288672hg38UCSC Ensembl
Outerchr5:67548601..67584500hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg3835900
hg1935900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997766
SamplesBILGI_BIOE
Known GenesPIK3R1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950077
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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