A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8733n54



Internal ID22776628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173511984..173592563hg38UCSC Ensembl
chr3:173229774..173310353hg19UCSC Ensembl
chr3:174712468..174793047hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3880580
hg1980580
hg1880580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592528, nsv592530, nsv592536, nsv592532, nsv592533, nsv592524, nsv592537, nsv592527, nsv592540, nsv592539
SamplesHGDP00857, HGDP00868, HGDP00336, HGDP00402, HGDP00709, HGDP00859
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8733n54
Frequency
Sample Size17421
Observed Gain26
Observed Loss0
Observed Complex0
Frequencyn/a


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