A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077913



Internal ID19319307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63339247..63340748hg38UCSC Ensembl
chr20:61970599..61972100hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765928
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077913
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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