A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545029



Internal ID16332438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1689422..1722233hg38UCSC Ensembl
Innerchr1:1620861..1653672hg19UCSC Ensembl
Innerchr1:1610720..1643532hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3832812
hg1932812
hg1832813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv39n54
Supporting Variantsnssv708618
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)nsv545029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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