A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010818



Internal ID19100035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103638263..103675085hg38UCSC Ensembl
Innerchr3:103357107..103393929hg19UCSC Ensembl
Innerchr3:104839797..104876619hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3836823
hg1936823
hg1836823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604379
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)nsv1010818
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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