A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014324



Internal ID19103545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403122..75500783hg38UCSC Ensembl
Innerchr3:75452273..75549934hg19UCSC Ensembl
Innerchr3:75534963..75632624hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3897662
hg1997662
hg1897662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4782n100
Supporting Variantsnssv3596129
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)nsv1014324
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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