A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv620n100



Internal ID20152236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248520087..248633900hg38UCSC Ensembl
chr1:248683388..248797201hg19UCSC Ensembl
chr1:246750011..246863824hg18UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38113814
hg19113814
hg18113814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011941, nsv1006457, nsv1001321, nsv1004960, nsv1013827, nsv1007110, nsv1005556, nsv1004141, nsv1005850, nsv1009314, nsv1012788
Samples
Known GenesOR2G6, OR2T10, OR2T11, OR2T29, OR2T34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv620n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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