A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954059



Internal ID16956246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:53576962..53590961hg38UCSC Ensembl
Outerchr20:52193501..52207500hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3814000
hg1914000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999995
SamplesBILGI_BIOE
Known GenesZNF217
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954059
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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