A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3908n100



Internal ID22789995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:87321364..87861756hg38UCSC Ensembl
chr2:87548487..88161275hg19UCSC Ensembl
chr2:87401998..87942390hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38540393
hg19612789
hg18540393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000368, nsv1001396, nsv1011417
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, 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)dgv3908n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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