A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077448



Internal ID19323854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:190093544..190119645hg38UCSC Ensembl
chr4:191014699..191040800hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3826102
hg1926102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763609
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077448
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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