A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1600n100



Internal ID22787687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18471488..18745495hg38UCSC Ensembl
chr13:19045628..19319635hg19UCSC Ensembl
chr13:17943628..18217635hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38274008
hg19274008
hg18274008
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040594, nsv1054001
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1600n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss6
Observed Complex0
Frequencyn/a


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