A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606476



Internal ID16047199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28534721..28535440hg38UCSC Ensembl
Innerchr7:28574339..28575058hg19UCSC Ensembl
Innerchr7:28540864..28541583hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg38720
hg19720
hg18720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11246n54
Supporting Variantsnssv1081562, nssv1081561
Samples
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606476
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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