A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11323n54



Internal ID22779218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:47049540..47052691hg38UCSC Ensembl
chr7:47089138..47092289hg19UCSC Ensembl
chr7:47055663..47058814hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg383152
hg193152
hg183152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606851, nsv606855, nsv606856
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11323n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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