A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766299



Internal ID18968768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10325257..10498658hg38UCSC Ensembl
chr21:11013799..11187200hg19UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38173402
hg19173402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078497
Supporting Variants
SamplesKWP1
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766299
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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