A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1256n100



Internal ID22787343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96479826..96553640hg38UCSC Ensembl
chr11:96212990..96286805hg19UCSC Ensembl
chr11:95852638..95926453hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3873815
hg1973816
hg1873816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044324, nsv1046903
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1256n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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