A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949777



Internal ID17298650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:6470974..6479673hg38UCSC Ensembl
Outerchr4:6472701..6481400hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996649
SamplesBILGI_BIOE
Known GenesPPP2R2C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949777
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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