A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545033



Internal ID16332442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1706566..1740343hg38UCSC Ensembl
Innerchr1:1638005..1671782hg19UCSC Ensembl
Innerchr1:1627865..1661642hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3833778
hg1933778
hg1833778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv40n54
Supporting Variantsnssv708627, nssv708626, nssv708625
Samples
Known GenesCDK11A, CDK11B, SLC35E2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545033
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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