A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077392



Internal ID18971586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8756766..8790067hg38UCSC Ensembl
chr21:9645599..9678900hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3833302
hg1933302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767676
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077392
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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