A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1721n100



Internal ID22787808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86416581..86482008hg38UCSC Ensembl
chr13:87068836..87134263hg19UCSC Ensembl
chr13:85866837..85932264hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3865428
hg1965428
hg1865428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052555, nsv1047019
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)dgv1721n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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