A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11495n54



Internal ID22779390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89891589..89903598hg38UCSC Ensembl
chr7:89520903..89532912hg19UCSC Ensembl
chr7:89358839..89370848hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3812010
hg1912010
hg1812010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607759, nsv607771, nsv607761, nsv607770, nsv607766, nsv607760
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11495n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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