A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv698n100



Internal ID22786785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28883965..28971225hg38UCSC Ensembl
chr10:29172894..29260154hg19UCSC Ensembl
chr10:29212900..29300160hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3887261
hg1987261
hg1887261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040780, nsv1043820
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)dgv698n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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