A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv681n100



Internal ID22786768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15884287..15906234hg38UCSC Ensembl
chr10:15926286..15948233hg19UCSC Ensembl
chr10:15966292..15988239hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3821948
hg1921948
hg1821948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053159, nsv1053577
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)dgv681n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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