A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013786



Internal ID19103005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75511382hg38UCSC Ensembl
Innerchr3:75427095..75560533hg19UCSC Ensembl
Innerchr3:75509785..75643223hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38133439
hg19133439
hg18133439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4776n100
Supporting Variantsnssv3602189, nssv3602190
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)nsv1013786
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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