A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608470



Internal ID16049193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137888441..137893015hg38UCSC Ensembl
Innerchr7:137573187..137577761hg19UCSC Ensembl
Innerchr7:137223727..137228301hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384575
hg194575
hg184575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094809, nssv1094810
Samples
Known GenesCREB3L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608470
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