A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11466n54



Internal ID19003642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76502756..76516897hg38UCSC Ensembl
chr7:76132073..76146214hg19UCSC Ensembl
chr7:75970009..75984150hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3814142
hg1914142
hg1814142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607590, nsv607592, nsv607589
Samples
Known GenesDTX2, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11466n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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