A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010289



Internal ID19099506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403122..75590743hg38UCSC Ensembl
Innerchr3:75452273..75639894hg19UCSC Ensembl
Innerchr3:75534963..75722584hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38187622
hg19187622
hg18187622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4784n100
Supporting Variantsnssv3596134, nssv3596131, nssv3596133, nssv3596132
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)nsv1010289
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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