A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545920



Internal ID15986643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28648638..28678234hg38UCSC Ensembl
Innerchr1:28975150..29004746hg19UCSC Ensembl
Innerchr1:28847737..28877333hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3829597
hg1929597
hg1829597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712053
Samples
Known GenesGMEB1, RNU11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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