A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999964



Internal ID16946230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33638795..33698694hg38UCSC Ensembl
Outerchr20:32226601..32286500hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3859900
hg1959900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954024
Supporting Variants
SamplesBILGI_BIOE
Known GenesACTL10, C20orf144, CBFA2T2, E2F1, NECAB3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999964
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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