A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589633



Internal ID16377042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8784337..8829531hg38UCSC Ensembl
Innerchr3:8826023..8871216hg19UCSC Ensembl
Innerchr3:8801023..8846216hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3845195
hg1945194
hg1845194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8215n54
Supporting Variantsnssv958875, nssv958872, nssv958874, nssv958876, nssv958873
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589633
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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