A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950032



Internal ID17298906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49205384..49324083hg38UCSC Ensembl
Outerchr4:49207401..49326100hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38118700
hg19118700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996709
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950032
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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