A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv879n100



Internal ID22786966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62274914..62368374hg38UCSC Ensembl
chr10:64034673..64128133hg19UCSC Ensembl
chr10:63704679..63798139hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3893461
hg1993461
hg1893461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050096, nsv1044761
Samples
Known GenesLOC283045
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv879n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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