A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118698



Internal ID19260267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:33672808..33677408hg38UCSC Ensembl
Outerchr3:33714300..33718900hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg384601
hg194601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959591
SamplesKWS1
Known GenesCLASP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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