A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766103



Internal ID19307957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122724683..122725984hg38UCSC Ensembl
chr10:124484199..124485500hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077322
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766103
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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