A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013514



Internal ID19102732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75632047hg38UCSC Ensembl
Innerchr3:75427095..75681198hg19UCSC Ensembl
Innerchr3:75509785..75763888hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38254104
hg19254104
hg18254104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4777n100
Supporting Variantsnssv3733687
Samples
Known GenesFAM86DP, MIR1324
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013514
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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