A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007266



Internal ID19096485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75500783hg38UCSC Ensembl
Innerchr3:75469493..75549934hg19UCSC Ensembl
Innerchr3:75552183..75632624hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3880442
hg1980442
hg1880442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4785n100
Supporting Variantsnssv3596142
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)nsv1007266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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