A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2609n100



Internal ID22788696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60025802..60062320hg38UCSC Ensembl
chr15:60318001..60354519hg19UCSC Ensembl
chr15:58105293..58141811hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3836519
hg1936519
hg1836519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043235, nsv1044105, nsv1045741
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)dgv2609n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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