A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv723n100



Internal ID20152339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43055119..43103915hg38UCSC Ensembl
chr10:43550567..43599363hg19UCSC Ensembl
chr10:42870573..42919369hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3848797
hg1948797
hg1848797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043295, nsv1041297, nsv1044759, nsv1045690, nsv1046759, nsv1039890
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)dgv723n100
Frequency
Sample Size29084
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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