A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3888n100



Internal ID19014256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87023361..87752799hg38UCSC Ensembl
chr2:87250484..88052318hg19UCSC Ensembl
chr2:87103995..87833433hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38729439
hg19801835
hg18729439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003146, nsv1006383, nsv1003093, nsv1009615, nsv1006634, nsv1007823, nsv1011527, nsv1002590, nsv1010975, nsv1007205, nsv1011714, nsv1001135, nsv1006012, nsv1014745, nsv1014950, nsv1003162
Samples
Known GenesLINC00152, LOC285074, 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)dgv3888n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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