A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545019



Internal ID16332428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1663759..1694348hg38UCSC Ensembl
Innerchr1:1595198..1625787hg19UCSC Ensembl
Innerchr1:1585061..1615647hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3830590
hg1930590
hg1830587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv37n54
Supporting Variantsnssv708606
Samples
Known GenesCDK11B, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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