A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv700n100



Internal ID22786787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29801849..29837823hg38UCSC Ensembl
chr10:30090778..30126752hg19UCSC Ensembl
chr10:30130784..30166758hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3835975
hg1935975
hg1835975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050467, nsv1040128, nsv1048762
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)dgv700n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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