A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589776



Internal ID16377185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:14600771..14629056hg38UCSC Ensembl
Innerchr3:14642278..14670563hg19UCSC Ensembl
Innerchr3:14617282..14645567hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3828286
hg1928286
hg1828286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151884
SamplesHGDP01296
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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