A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545853



Internal ID15986576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25284602..25313871hg38UCSC Ensembl
Innerchr1:25611093..25640362hg19UCSC Ensembl
Innerchr1:25483680..25512949hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3829270
hg1929270
hg1829270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv206n54
Supporting Variantsnssv711789, nssv711790
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545853
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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