A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954018



Internal ID17302892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:30310625..30404124hg38UCSC Ensembl
Outerchr20:29545301..29638800hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3893500
hg1993500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999958
SamplesBILGI_BIOE
Known GenesFRG1B, MLLT10P1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954018
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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