A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110409



Internal ID18906985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:43011708..43017908hg38UCSC Ensembl
Outerchr3:43053200..43059400hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386201
hg196201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960060
SamplesKWS1
Known GenesFAM198A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110409
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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