A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591198



Internal ID16378607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103382907..103461553hg38UCSC Ensembl
Innerchr3:103101751..103180397hg19UCSC Ensembl
Innerchr3:104584441..104663087hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3878647
hg1978647
hg1878647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8485n54
Supporting Variantsnssv970926
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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