A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955147



Internal ID17304020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:62047545..62059044hg38UCSC Ensembl
Outerchr20:60622601..60634100hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000009
SamplesBILGI_BIOE
Known GenesTAF4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955147
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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