A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1018n100



Internal ID22787105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3395247..3597187hg38UCSC Ensembl
chr11:3416477..3618417hg19UCSC Ensembl
chr11:3373053..3574993hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38201941
hg19201941
hg18201941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042782, nsv1036243, nsv1051536, nsv1050289, nsv1042884, nsv1048775, nsv1048017, nsv1043863, nsv1047360, nsv1050993, nsv1047674
Samples
Known GenesLOC650368
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1018n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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