A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3861n100



Internal ID20155477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64115335..64290325hg38UCSC Ensembl
chr2:64342469..64517459hg19UCSC Ensembl
chr2:64195973..64370963hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38174991
hg19174991
hg18174991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999608, nsv1000390, nsv1015084, nsv1012905, nsv1013735
Samples
Known GenesLINC00309, PELI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3861n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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