A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074706



Internal ID18969489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40344415..40347891hg38UCSC Ensembl
chr4:40346432..40349908hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg383477
hg193477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769683
SamplesKWP1
Known GenesCHRNA9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074706
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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