A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1136n100



Internal ID22787223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50101766..50699606hg38UCSC Ensembl
chr11:50060937..50658777hg19UCSC Ensembl
chr11:50017513..50615353hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38597841
hg19597841
hg18597841
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051675, nsv1051055, nsv1035641, nsv1035439, nsv1042046, nsv1049947, nsv1047502, nsv1041731, nsv1053769
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1136n100
Frequency
Sample Size11257
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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