A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009873



Internal ID19099092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75445265hg38UCSC Ensembl
Innerchr3:75427095..75494416hg19UCSC Ensembl
Innerchr3:75509785..75577106hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3867322
hg1967322
hg1867322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4780n100
Supporting Variantsnssv3733031, nssv3602007, nssv3602003, nssv3602002, nssv3602004, nssv3733030, nssv3602006, nssv3602008, nssv3602005
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)nsv1009873
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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