A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv877n100



Internal ID22786964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58076728..58120472hg38UCSC Ensembl
chr10:59836488..59880233hg19UCSC Ensembl
chr10:59506494..59550239hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3843745
hg1943746
hg1843746
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037201, nsv1039348, nsv1044158
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)dgv877n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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