A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009339



Internal ID19098557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:86624023..86676563hg38UCSC Ensembl
Innerchr3:86673173..86725713hg19UCSC Ensembl
Innerchr3:86755863..86808403hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3852541
hg1952541
hg1852541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596275
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)nsv1009339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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