A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3887n100



Internal ID19014255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:86878321..87752799hg38UCSC Ensembl
chr2:87105444..88052318hg19UCSC Ensembl
chr2:86958955..87833433hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38874479
hg19946875
hg18874479
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997663, nsv1010107
Samples
Known GenesANAPC1P1, LINC00152, LOC285074, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, PLGLB1, PLGLB2, RGPD1, RGPD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3887n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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