A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954061



Internal ID17302935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:53651262..53661761hg38UCSC Ensembl
Outerchr20:52267801..52278300hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999996
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954061
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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