A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001606



Internal ID19090823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75500555hg38UCSC Ensembl
Innerchr3:75427095..75549706hg19UCSC Ensembl
Innerchr3:75509785..75632396hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38122612
hg19122612
hg18122612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3602151, nssv3602150
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)nsv1001606
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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