A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771311



Internal ID19307894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8534566..8547767hg38UCSC Ensembl
chr21:9423399..9436600hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3813202
hg1913202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077389
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771311
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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