A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv875n100



Internal ID22786962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57503097..57592998hg38UCSC Ensembl
chr10:59262857..59352758hg19UCSC Ensembl
chr10:58932863..59022764hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3889902
hg1989902
hg1889902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052321, nsv1043592
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)dgv875n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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