A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1229n100



Internal ID19011597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76948433..77017224hg38UCSC Ensembl
chr11:76659477..76728268hg19UCSC Ensembl
chr11:76337125..76405916hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3868792
hg1968792
hg1868792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040833, nsv1042924
Samples
Known GenesACER3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1229n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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