A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003560



Internal ID19092778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75413466..75511978hg38UCSC Ensembl
Innerchr3:75462617..75561129hg19UCSC Ensembl
Innerchr3:75545307..75643819hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3898513
hg1998513
hg1898513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596138
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)nsv1003560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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