A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960070



Internal ID19220885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:169676712..169685212hg38UCSC Ensembl
Outerchr3:169394500..169403000hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg388501
hg198501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110419
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960070
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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