A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv876n100



Internal ID22786963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58075195..58136187hg38UCSC Ensembl
chr10:59834955..59895948hg19UCSC Ensembl
chr10:59504961..59565954hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3860993
hg1960994
hg1860994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048212, nsv1052651, nsv1048143, nsv1050824, nsv1047908, nsv1046635
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv876n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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