A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4986n100



Internal ID22791073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173522833..173590561hg38UCSC Ensembl
chr3:173240623..173308351hg19UCSC Ensembl
chr3:174723317..174791045hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3867729
hg1967729
hg1867729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009921, nsv1005121, nsv1002335, nsv1008730
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4986n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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