A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv867n100



Internal ID22786954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55679434..55971344hg38UCSC Ensembl
chr10:57439194..57731104hg19UCSC Ensembl
chr10:57109200..57401110hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38291911
hg19291911
hg18291911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035651, nsv1038525
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)dgv867n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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