A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950034



Internal ID17298908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49486984..49520083hg38UCSC Ensembl
Outerchr4:49489001..49522100hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3833100
hg1933100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996711
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950034
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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