A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2610n100



Internal ID22788697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60172801..60238144hg38UCSC Ensembl
chr15:60465000..60530343hg19UCSC Ensembl
chr15:58252292..58317635hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3865344
hg1965344
hg1865344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039861, nsv1049553, nsv1036168
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)dgv2610n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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