A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3900n100



Internal ID22789987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87146758..87752799hg38UCSC Ensembl
chr2:87373881..88052318hg19UCSC Ensembl
chr2:87227392..87833433hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38606042
hg19678438
hg18606042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004785, nsv999557, nsv1004397, nsv1006980, nsv1009468, nsv999371, nsv1006325, nsv998146, nsv1008411, nsv997620, nsv1004232, nsv1009126, nsv1011092, nsv1003315, nsv1001592, nsv1006464, nsv998540, nsv1011195, nsv1012100, nsv1014273, nsv1003347, nsv1014082, nsv1001966, nsv1007299, nsv1003037, nsv1002857, nsv998494, nsv1013688, nsv1003193
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2, PLGLB1, PLGLB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3900n100
Frequency
Sample Size11257
Observed Gain43
Observed Loss0
Observed Complex0
Frequencyn/a


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