A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589995



Internal ID16377404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26391597..26410722hg38UCSC Ensembl
Innerchr3:26433088..26452213hg19UCSC Ensembl
Innerchr3:26408092..26427217hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819126
hg1919126
hg1819126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv960375
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589995
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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