A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591201



Internal ID16378610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103461553..103589916hg38UCSC Ensembl
Innerchr3:103180397..103308760hg19UCSC Ensembl
Innerchr3:104663087..104791450hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38128364
hg19128364
hg18128364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8487n54
Supporting Variantsnssv970929, nssv970928
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591201
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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