A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv474n100



Internal ID20152090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180152345..180273524hg38UCSC Ensembl
chr1:180121480..180242659hg19UCSC Ensembl
chr1:178388103..178509282hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38121180
hg19121180
hg18121180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012145, nsv999182, nsv1002133, nsv1005512, nsv999104, nsv1007590
Samples
Known GenesFLJ23867, LHX4, LOC100527964, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv474n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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