A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2577n100



Internal ID22788664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38826062..38867666hg38UCSC Ensembl
chr15:39118263..39159867hg19UCSC Ensembl
chr15:36905555..36947159hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3841605
hg1941605
hg1841605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046027, nsv1039615
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)dgv2577n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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