A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953309



Internal ID16955496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63938748..63978447hg38UCSC Ensembl
Outerchr20:62570101..62609800hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3839700
hg1939700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000020
SamplesBILGI_BIOE
Known GenesMIR1914, MIR647, SAMD10, UCKL1, UCKL1-AS1, ZNF512B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953309
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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