A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139742



Internal ID19260997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:197635176..197640676hg38UCSC Ensembl
Outerchr2:198499900..198505400hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg385501
hg195501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978081
SamplesKWS2
Known GenesRFTN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139742
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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