A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981120



Internal ID15928390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164547652..165237953hg38UCSC Ensembl
Innerchr3:164265440..164955741hg19UCSC Ensembl
Innerchr3:165748134..166438435hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38690302
hg19690302
hg18690302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592446
Supporting Variants
Samples
Known GenesSI, SLITRK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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