A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766956



Internal ID19309827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9922271..9995872hg38UCSC Ensembl
chr21:10400299..10473900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3873602
hg1973602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078495
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766956
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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