A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2679n100



Internal ID22788766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101611117..101675562hg38UCSC Ensembl
chr15:102151320..102215765hg19UCSC Ensembl
chr15:99968843..100033288hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3864446
hg1964446
hg1864446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052841, nsv1050400, nsv1053474
Samples
Known GenesTARSL2, TM2D3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2679n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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