A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1202n54



Internal ID22769097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63521170..63521923hg38UCSC Ensembl
chr10:65280930..65281683hg19UCSC Ensembl
chr10:64950936..64951689hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38754
hg19754
hg18754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551186, nsv551185
Samples
Known GenesREEP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1202n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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