A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1258n100



Internal ID22787345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97107874..97237386hg38UCSC Ensembl
chr11:96978874..97108386hg19UCSC Ensembl
chr11:96484084..96613596hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38129513
hg19129513
hg18129513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047823, nsv1042769, nsv1046583, nsv1051822
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)dgv1258n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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