A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952967



Internal ID16955154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:668557..676856hg38UCSC Ensembl
Outerchr20:649201..657500hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg388300
hg198300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999903
SamplesBILGI_BIOE
Known GenesSCRT2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952967
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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