A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1224n100



Internal ID22787311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71712419..71816653hg38UCSC Ensembl
chr11:71423465..71527699hg19UCSC Ensembl
chr11:71101113..71205347hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38104235
hg19104235
hg18104235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043197, nsv1037092
Samples
Known GenesALG1L9P, FAM86C1, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1224n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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