A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545923



Internal ID16333332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:29446528..29457243hg38UCSC Ensembl
Innerchr1:29773040..29783755hg19UCSC Ensembl
Innerchr1:29645627..29656342hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg3810716
hg1910716
hg1810716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv712055
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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