A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075821



Internal ID19326220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47666379..47676580hg38UCSC Ensembl
chr10:47356399..47366600hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3810202
hg1910202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763542
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075821
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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