A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013299



Internal ID19102517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75434082..75497567hg38UCSC Ensembl
Innerchr3:75483233..75546718hg19UCSC Ensembl
Innerchr3:75565923..75629408hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3863486
hg1963486
hg1863486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4785n100
Supporting Variantsnssv3596153
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013299
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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