A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv249n100



Internal ID22786336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108103935..108121219hg38UCSC Ensembl
chr1:108646557..108663841hg19UCSC Ensembl
chr1:108448080..108465364hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817285
hg1917285
hg1817285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1002206, nsv1002495
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv249n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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