A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545919



Internal ID15986642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28501377..28511063hg38UCSC Ensembl
Innerchr1:28827889..28837575hg19UCSC Ensembl
Innerchr1:28700476..28710162hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg389687
hg199687
hg189687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712052
Samples
Known GenesRCC1, SNHG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545919
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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