A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997798



Internal ID18810648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3858107..4053010hg38UCSC Ensembl
Innerchr3:3899791..4094694hg19UCSC Ensembl
Innerchr3:3874791..4069694hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38194904
hg19194904
hg18194904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4638n100
Supporting Variantsnssv3590389
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997798
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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