A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014979



Internal ID19104196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75497567hg38UCSC Ensembl
Innerchr3:75421158..75546718hg19UCSC Ensembl
Innerchr3:75503848..75629408hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38125561
hg19125561
hg18125561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3732994
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)nsv1014979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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