A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1253n100



Internal ID20152869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93153482..93181889hg38UCSC Ensembl
chr11:92886648..92915055hg19UCSC Ensembl
chr11:92526296..92554703hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3828408
hg1928408
hg1828408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045544, nsv1047828, nsv1041794
Samples
Known GenesSLC36A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1253n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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