A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003260



Internal ID19092478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75482049hg38UCSC Ensembl
Innerchr3:75427095..75531200hg19UCSC Ensembl
Innerchr3:75509785..75613890hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38104106
hg19104106
hg18104106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3602033
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)nsv1003260
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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