A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11719n54



Internal ID20145143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150856387..150875294hg38UCSC Ensembl
chr7:150553475..150572382hg19UCSC Ensembl
chr7:150184408..150203315hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3818908
hg1918908
hg1818908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608996, nsv608994, nsv608995
Samples
Known GenesAOC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11719n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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