A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1645n100



Internal ID22787732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:47505382..47530647hg38UCSC Ensembl
chr13:48079517..48104782hg19UCSC Ensembl
chr13:46977518..47002783hg18UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3825266
hg1925266
hg1825266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041047, nsv1043543
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)dgv1645n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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