A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3891n100



Internal ID22789978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87094919..87598258hg38UCSC Ensembl
chr2:87322042..87897777hg19UCSC Ensembl
chr2:87175553..87678892hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38503340
hg19575736
hg18503340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998306, nsv999034, nsv1011829, nsv1009090, nsv1010524, nsv1001754, nsv998393, nsv1006683, nsv1000333, nsv1003251, nsv1004684, nsv1007569
Samples
Known GenesLINC00152, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3891n100
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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