A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv298n100



Internal ID22786385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:118652982..118677873hg38UCSC Ensembl
chr1:119195605..119220496hg19UCSC Ensembl
chr1:118997128..119022019hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3824892
hg1924892
hg1824892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009731, nsv997474, nsv1001997
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)dgv298n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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