A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076369



Internal ID18972466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131916595..131918996hg38UCSC Ensembl
chr10:133730099..133732500hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765999
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076369
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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