A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005864



Internal ID19095081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75481824hg38UCSC Ensembl
Innerchr3:75427095..75530975hg19UCSC Ensembl
Innerchr3:75509785..75613665hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38103881
hg19103881
hg18103881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3602032
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)nsv1005864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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