A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv697n100



Internal ID19011065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28275066..28285695hg38UCSC Ensembl
chr10:28563995..28574624hg19UCSC Ensembl
chr10:28604001..28614630hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3810630
hg1910630
hg1810630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036270, nsv1045247
Samples
Known GenesMPP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv697n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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