A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11662n54



Internal ID22779557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143130861..143174945hg38UCSC Ensembl
chr7:142827954..142872038hg19UCSC Ensembl
chr7:142538076..142582160hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3844085
hg1944085
hg1844085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608669, nsv608661, nsv608660
Samples
Known GenesPIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11662n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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