A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1156n100



Internal ID22787243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54762047..54852259hg38UCSC Ensembl
chr11:51267021..51357233hg19UCSC Ensembl
chr11:51123597..51213809hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3890213
hg1990213
hg1890213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040549, nsv1040561, nsv1044703, nsv1042152
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)dgv1156n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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