A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606470



Internal ID16047193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28448634..28512759hg38UCSC Ensembl
Innerchr7:28488252..28552377hg19UCSC Ensembl
Innerchr7:28454777..28518902hg18UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3864126
hg1964126
hg1864126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154927
SamplesHGDP00444
Known GenesCREB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606470
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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