A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006386



Internal ID18748917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4104499..4153986hg38UCSC Ensembl
Innerchr3:4146183..4195670hg19UCSC Ensembl
Innerchr3:4121183..4170670hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3849488
hg1949488
hg1849488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4651n100
Supporting Variantsnssv3590464
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)nsv1006386
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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