A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1017n100



Internal ID22787104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3388929..3607794hg38UCSC Ensembl
chr11:3410159..3629024hg19UCSC Ensembl
chr11:3366735..3585600hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38218866
hg19218866
hg18218866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045606, nsv1042319, nsv1040226, nsv1047150, nsv1052574, nsv1048151, nsv1039294
Samples
Known GenesLOC650368, OR7E12P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1017n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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