A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999390



Internal ID19158926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75366712..75625450hg38UCSC Ensembl
Innerchr3:75415863..75674601hg19UCSC Ensembl
Innerchr3:75498553..75757291hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38258739
hg19258739
hg18258739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3594961
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)nsv999390
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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