A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544933



Internal ID15985656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:934429..943937hg38UCSC Ensembl
Innerchr1:869809..879317hg19UCSC Ensembl
Innerchr1:859672..869180hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389509
hg199509
hg189509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n54
Supporting Variantsnssv708451
Samples
Known GenesSAMD11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544933
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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