A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11718n54



Internal ID22779613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:150338437..150418095hg38UCSC Ensembl
chr7:150035526..150115183hg19UCSC Ensembl
chr7:149666459..149746116hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3879659
hg1979658
hg1879658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608992, nsv608991
Samples
Known GenesLOC728743, RARRES2, REPIN1, RNU6-33P, RNU6-34P, ZNF775
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11718n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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