A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11119n54



Internal ID22779014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1121522..1185274hg38UCSC Ensembl
chr7:1161158..1224910hg19UCSC Ensembl
chr7:1127684..1191436hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3863753
hg1963753
hg1863753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605736, nsv605737
Samples
Known GenesC7orf50, ZFAND2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11119n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer