A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589412



Internal ID16376821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4034049..4062242hg38UCSC Ensembl
Innerchr3:4075733..4103926hg19UCSC Ensembl
Innerchr3:4050733..4078926hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3828194
hg1928194
hg1828194
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8176n54
Supporting Variantsnssv958006
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589412
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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