A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589524



Internal ID16376933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6583394..6612373hg38UCSC Ensembl
Innerchr3:6625081..6654060hg19UCSC Ensembl
Innerchr3:6600081..6629060hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3828980
hg1928980
hg1828980
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8196n54
Supporting Variantsnssv958280, nssv958279
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589524
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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