A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978081



Internal ID19241952
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 StatusS
Merged Variantsnsv1139742
Supporting Variants
SamplesKWS2
Known GenesRFTN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978081
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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