A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545021



Internal ID15985744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1663759..1713469hg38UCSC Ensembl
Innerchr1:1595198..1644908hg19UCSC Ensembl
Innerchr1:1585061..1634768hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3849711
hg1949711
hg1849708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38n54
Supporting Variantsnssv708609
Samples
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545021
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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