A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3893n100



Internal ID22789980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87094919..87936285hg38UCSC Ensembl
chr2:87322042..88235804hg19UCSC Ensembl
chr2:87175553..88016919hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38841367
hg19913763
hg18841367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006743, nsv1001901, nsv1012801, nsv1010878, nsv1004867, nsv998193, nsv1002059, nsv1000228
Samples
Known GenesLINC00152, 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)dgv3893n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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