A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv983n100



Internal ID22787070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121669087..121692680hg38UCSC Ensembl
chr10:123428601..123452194hg19UCSC Ensembl
chr10:123418591..123442184hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823594
hg1923594
hg1823594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048906, nsv1036499
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)dgv983n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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