A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009495



Internal ID19098713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75537642hg38UCSC Ensembl
Innerchr3:75469493..75586793hg19UCSC Ensembl
Innerchr3:75552183..75669483hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38117301
hg19117301
hg18117301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4783n100
Supporting Variantsnssv3596144, nssv3596143
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)nsv1009495
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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