A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954014



Internal ID17302888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:26277965..26338864hg38UCSC Ensembl
Outerchr20:26258601..26319500hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3860900
hg1960900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999955
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954014
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer