A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv950n100



Internal ID22787037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89178404..89197932hg38UCSC Ensembl
chr10:90938161..90957689hg19UCSC Ensembl
chr10:90928141..90947669hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3819529
hg1919529
hg1819529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051861, nsv1049521
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)dgv950n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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