A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv919n100



Internal ID20152535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68400084..68752800hg38UCSC Ensembl
chr10:70159841..70512557hg19UCSC Ensembl
chr10:69829847..70182563hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38352717
hg19352717
hg18352717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051520, nsv1051944, nsv1049834
Samples
Known GenesCCAR1, DNA2, RUFY2, SLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv919n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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