A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv949n100



Internal ID22787036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87212064..87435973hg38UCSC Ensembl
chr10:88971821..89195730hg19UCSC Ensembl
chr10:88961801..89185710hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38223910
hg19223910
hg18223910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048272, nsv1040693
Samples
Known GenesLINC00864, LOC439994, NUTM2A, NUTM2A-AS1, NUTM2D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv949n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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