A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1627n100



Internal ID22787714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37490980..37510608hg38UCSC Ensembl
chr13:38065117..38084745hg19UCSC Ensembl
chr13:36963117..36982745hg18UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3819629
hg1919629
hg1819629
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053772, nsv1053615
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)dgv1627n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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