A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767124



Internal ID19307421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133782774..133787422hg38UCSC Ensembl
chr10:135520099..135524800hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg384649
hg194702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077326
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767124
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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