A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv635n100



Internal ID20152251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248585881..248650779hg38UCSC Ensembl
chr1:248749182..248814080hg19UCSC Ensembl
chr1:246815805..246880703hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3864899
hg1964899
hg1864899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997868, nsv1009248, nsv1010035, nsv1007867, nsv1007075, nsv1003586, nsv998342, nsv1008410, nsv1011570, nsv1013857, nsv999467, nsv1007594
Samples
Known GenesOR2T10, OR2T11, OR2T27, OR2T35
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv635n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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