A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999914



Internal ID16946180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:2835355..2842754hg38UCSC Ensembl
Outerchr20:2816001..2823400hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952978
Supporting Variants
SamplesBILGI_BIOE
Known GenesPCED1A, VPS16
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999914
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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