A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608467



Internal ID16049190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137888388..137888862hg38UCSC Ensembl
Innerchr7:137573134..137573608hg19UCSC Ensembl
Innerchr7:137223674..137224148hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38475
hg19475
hg18475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11621n54
Supporting Variantsnssv1094790
Samples
Known GenesCREB3L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608467
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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