A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv874n100



Internal ID22786961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57069923..57111825hg38UCSC Ensembl
chr10:58829683..58871585hg19UCSC Ensembl
chr10:58499689..58541591hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3841903
hg1941903
hg1841903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037860, nsv1054466, nsv1043708
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)dgv874n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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