A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954029



Internal ID16956216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35284398..35298997hg38UCSC Ensembl
Outerchr20:33872201..33886800hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3814600
hg1914600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999968
SamplesBILGI_BIOE
Known GenesEIF6, FAM83C
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954029
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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