A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv707n100



Internal ID20152323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35130935..35383078hg38UCSC Ensembl
chr10:35419863..35672006hg19UCSC Ensembl
chr10:35459869..35712012hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38252144
hg19252144
hg18252144
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046451, nsv1035644, nsv1050733
Samples
Known GenesCCNY, CREM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv707n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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