A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1222n100



Internal ID20152838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71582829..71827945hg38UCSC Ensembl
chr11:71293875..71538991hg19UCSC Ensembl
chr11:70971523..71216639hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38245117
hg19245117
hg18245117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051879, nsv1035306, nsv1037088, nsv1036258, nsv1041027, nsv1044041
Samples
Known GenesALG1L9P, FAM86C1, KRTAP5-11, ZNF705E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1222n100
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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