A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014160



Internal ID19103380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197065763..197130801hg38UCSC Ensembl
Innerchr3:196792634..196857672hg19UCSC Ensembl
Innerchr3:198277031..198342069hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3865039
hg1965039
hg1865039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3617006
Samples
Known GenesDLG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014160
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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