A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2611n100



Internal ID22788698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60229106..60260552hg38UCSC Ensembl
chr15:60521305..60552751hg19UCSC Ensembl
chr15:58308597..58340043hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3831447
hg1931447
hg1831447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036994, nsv1038350
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)dgv2611n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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