A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768775



Internal ID19312083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4227651..4227704hg38UCSC Ensembl
chr20:4208298..4208351hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072099
Supporting Variants
SamplesKWP1
Known GenesADRA1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768775
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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