A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596142



Internal ID18894423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75420342..75500783hg38UCSC Ensembl
Innerchr3:75469493..75549934hg19UCSC Ensembl
Innerchr3:75552183..75632624hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3880442
hg1980442
hg1880442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007266
Supporting Variants
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)nssv3596142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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