A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11465n54



Internal ID19003641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76482621..76885926hg38UCSC Ensembl
chr7:76111938..76515243hg19UCSC Ensembl
chr7:75949874..76353179hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38403306
hg19403306
hg18403306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607616, nsv607591, nsv607587, nsv607615, nsv607614
Samples
Known GenesDTX2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11465n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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