A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv727n100



Internal ID20152343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43083220..43096898hg38UCSC Ensembl
chr10:43578668..43592346hg19UCSC Ensembl
chr10:42898674..42912352hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3813679
hg1913679
hg1813679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050957, nsv1051682, nsv1054078, nsv1042400, nsv1040004, nsv1052444
Samples
Known GenesRET
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv727n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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