A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv853n100



Internal ID19011221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50014227..50407682hg38UCSC Ensembl
chr10:51773987..52167442hg19UCSC Ensembl
chr10:51443993..51837448hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38393456
hg19393456
hg18393456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051028, nsv1053903, nsv1040661, nsv1037118
Samples
Known GenesASAH2, FAM21A, FAM21B, FLJ31813, SGMS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv853n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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